New Indications and Dosage Forms for Existing Medications

Drugs that have gained FDA approval for the treatment of additional diseases/conditions or new dosage forms/regimens.

New Indications and Dosage Forms

Cardene (nicardipine)

Date of Approval: December 21, 1988

Cardene (nicardipine) is a calcium channel blocker for the treatment of hypertension and angina.

New Formulation Approved: November 7, 2008


Premarin Vaginal Cream (conjugated estrogens)

Date of Approval: October 16, 1978

Premarin Vaginal Cream is a vaginal estrogen therapy indicated for the treatment of atrophic vaginitis, kraurosis vulvae and the treatment of moderate to severe dyspareunia, a symptom of vulvar and vaginal atrophy due to menopause.

New Indication Approved: November 7, 2008


Crestor (rosuvastatin calcium)

Date of Approval: August 12, 2003

Crestor is a HMG-CoA reductase inhibitor approved as an adjunct to diet for the treatment of various lipid disorders including primary hypercholesterolemia, mixed dyslipidemia and isolated hypertriglyceridemia.

New Indication Approved: November 6, 2008


Ranexa (ranolazine)

Date of Approval: January 27, 2006

Ranexa is an antianginal and anti-ischemic agent indicated for the treatment of chronic angina.

New Indication Approved: November 5, 2008


Treanda (bendamustine hydrochloride)

Date of Approval: March 20, 2008

Treanda (bendamustine) is a purine alkylator hybrid chemotherapy agent indicated for the treatment of patients with chronic lymphocytic leukemia (CLL) and relapsed indolent non-Hodgkin's lymphoma.

New Indication Approved: October 31, 2008


Apidra (insulin glulisine)

Date of Approval: April 16, 2004

Apidra is a rapid-acting recombinant DNA human insulin analogue used for the control of hyperglycemia in patients with diabetes mellitus.

Patient Population Altered: October 24, 2008


Prezista (darunavir)

Date of Approval: June 23, 2006

Prezista is a protease inhibitor used with ritonavir in combination with other antiretroviral agents for the treatment of human immunodeficiency virus (HIV) infection.

Patient Population Altered: October 21, 2008


Focalin XR (dexmethylphenidate)

Date of Approval: May 26, 2005

Focalin XR is a once-daily extended-release form of Focalin indicated for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD) in adults, adolescents and children.

Labeling Revision Approved: October 17, 2008


Risperdal (risperidone)

Date of Approval: December 29, 1993

Risperdal (risperidone) is an atypical antipsychotic agent indicated for the treatment of schizophrenia, acute manic or mixed episodes associated with Bipolar I Disorder and the treatment of irritability associated with autistic disorder.

New Dosage Regimen: October 10, 2008


Seroquel (quetiapine)

Date of Approval: September 26, 1997

Seroquel (quetiapine) is a psychotropic agent used to treat the symptoms of psychotic conditions such as schizophrenia and bipolar disorder.

New Indication Approved: October 8, 2008


Vaprisol (conivaptan hydrochloride)

Date of Approval: December 29, 2005

Vaprisol (conivaptan hydrochloride injection) is an arginine vasopressin antagonist for the treatment of euvolemic and hypervolemic hyponatremia in hospitalized patients.

New Formulation Approved: October 8, 2008


Reyataz (atazanavir sulfate)

Date of Approval: June 20, 2003

Reyataz is a protease inhibitor indicated for use in combination with other antiretroviral agents for the treatment of HIV-1 infection.

Patient Population Altered: September 30, 2008


Alimta (pemetrexed)

Date of Approval: February 4, 2004

Alimta is an antifolate antineoplastic agent indicated for the treatment of malignant pleural mesothelioma and locally-advanced and metastatic non-small cell lung cancer (NSCLC).

New Indication Approved: September 26, 2008


Nasacort (triamcinolone acetonide)

Date of Approval: July 11, 1991

Nasacort (triamcinolone acetonide) is an intranasal corticosteroid indicated for the treatment of nasal symptoms associated with seasonal and perennial allergic rhinitis.

Patient Population Altered: September 19, 2008


ProAir HFA (albuterol sulfate)

Date of Approval: October 29, 2004

ProAir HFA (albuterol sulfate) inhalation aerosol is a beta2-adrenergic agonist indicated for treatment or prevention of bronchospasm.

Patient Population Altered: September 16, 2008


Gardasil (human papillomavirus quadrivalent (types 6, 11, 16, and 18) vaccine, recombinant)

Date of Approval: June 8, 2006

Gardasil is a recombinant vaccine indicated for the prevention of cervical, vulvar, and vaginal cancers caused by human papillomavirus in girls and women 9 through 26 years of age.

New Indication Approved: September 12, 2008


Gamunex (immune globulin intravenous (human))

Date of Approval: August 27, 2003

Gamunex (immune globulin intravenous (human)) is indicated for the treatment of primary humoral immunodeficiency, idiopathic thrombocytopenic purpura and chronic inflammatory demyelinating polyneuropathy (CIDP).

New Indication Approved: September 12, 2008


Keppra (levetiracetam)

Date of Approval: November 30, 1999

Keppra is an antiepileptic drug used to treat partial onset seizures in people with epilepsy. It is also used to treat myoclonic seizures and tonic-clonic seizures.

New Dosage Form Approved: September 12, 2008


Novolog Mix (insulin aspart and insulin aspart protamine)

Date of Approval: November 1, 2001

Novolog Mix (insulin aspart and insulin aspart protamine) is an insulin combination used to treat type 1 (insulin-dependent) diabetes in adults.

New Formulation Approved: August 26, 2008


Omnitrope (somatropin (rDNA origin))

Date of Approval: May 30, 2006

Omnitrope is a recombinant human growth hormone indicated for treatment of children with growth failure due to growth hormone deficiency GHD and treatment of adults with either adult onset or childhood onset GHD.

New Formulation Approved: August 25, 2008


Aloxi (palonosetron)

Date of Approval: July 25, 2003

Aloxi is a 5-HT3 receptor antagonist indicated for the prevention of nausea and vomiting associated with chemotherapy.

New Dosage Form Approved: August 22, 2008


Vidaza (azacitidine)

Date of Approval: May 19, 2004

Vidaza (azacitidine) is an antineoplastic agent for the treatment of patients with myelodysplastic syndromes.

New Indication Approved: August 20, 2008


Viread (tenofovir disoproxil fumarate)

Date of Approval: October 26, 2001

Viread (tenofovir disoproxil fumarate) is a nucleoside reverse transcriptase inhibitor (NRTI) for the treatment of HIV infection and chronic hepatitis B in adults.

New Indication Approved: August 11, 2008


Cardene (nicardipine)

Date of Approval: December 21, 1988

Cardene (nicardipine) is a calcium channel blocker for the treatment of hypertension and angina.

New Formulation Approved: July 31, 2008


Exforge (amlodipine and valsartan)

Date of Approval: June 20, 2007

Exforge is a single-tablet combination of an angiotensin receptor blocker (valsartan) and a calcium channel blocker (amlodipine) taken once-daily for the treatment of hypertension.

New Indication Approved: July 23, 2008


Requip (ropinirole)

Date of Approval: September 19, 1997

Requip (ropinirole) is a non-ergoline dopamine agonist indicated for the treatment of the signs and symptoms of idiopathic Parkinson’s disease.

New Dosage Form Approved: July 1, 2008


Aciphex (rabeprazole)

Date of Approval: August 19, 1999

Aciphex (rabeprazole) is a proton-pump inhibitor indicated for the treatment of gastroesophageal reflux disease (GERD) and other conditions involving excessive stomach acid.

Patient Population Altered: June 30, 2008


Concerta (methylphenidate)

Date of Approval: August 1, 2000

Concerta (methylphenidate) is a central nervous system (CNS) stimulant indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in children 6 years of age and older, adolescents, and adults up to the age of 65.

Patient Population Altered: June 27, 2008


Metvixia (methyl aminolevulinate hydrochloride)

Date of Approval: July 27, 2004

Metvixia is a non-invasive treatment which combines the local application of cream and illumination with a proprietary red light source (CureLight/Aktilite) to activate the drug for the photodynamic treatment of sun-induced pre-cancerous skin lesions (actinic keratosis).

New Formulation Approved: June 26, 2008


Aptivus (tipranavir)

Date of Approval: June 22, 2005

Aptivus is a non-peptidic protease inhibitor which is co-administered with ritonavir for the treatment of HIV Infection.

New Dosage Form Approved: June 23, 2008


Velcade (bortezomib)

Date of Approval: May 13, 2003

Velcade is an antineoplastic agent indicated for the treatment of multiple myeloma.

New Indication Approved: June 20, 2008


Avodart (dutasteride)

Date of Approval: November 20, 2001

Avodart (dutasteride) is a 5á-reductase inhibitor indicated for the treatment of symptomatic benign prostatic hyperplasia (BPH).

New Indication Approved: June 19, 2008


Cymbalta (duloxetine)

Date of Approval: August 3, 2004

Cymbalta is a selective serotonin and norepinephrine reuptake inhibitor (SSNRI). Cymbalta is indicated for the treatment of major depressive disorder, neuropathic pain associated with diabetic peripheral neuropathy, generalized anxiety disorder and fibromyalgia.

New Indication Approved: June 13, 2008


Reclast (zoledronic acid)

Date of Approval: April 16, 2007

Reclast is a bisphosphonate indicated for the treatment for Paget's disease, postmenopausal osteoporosis and prevention of fractures.

New Indication Approved: June 3, 2008


Seroquel (quetiapine)

Date of Approval: September 26, 1997

Seroquel (quetiapine) is a psychotropic agent used to treat the symptoms of psychotic conditions such as schizophrenia and bipolar disorder.

New Indication Approved: May 13, 2008


Taclonex (calcipotriene and betamethasone dipropionate)

Date of Approval: January 9, 2006

Taclonex is a topical ointment containing a combination of calcipotriene and betamethasone for the treatment of psoriasis vulgaris in adults.

New Dosage Form Approved: May 9, 2008


Strattera (atomoxetine)

Date of Approval: November 26, 2002

Strattera is a selective norepinephrine reuptake inhibitor indicated for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD).

New Indication Approved: May 7, 2008


Abilify (aripiprazole)

Date of Approval: November 15, 2002

Abilify (aripiprazole) is a psychotropic drug indicated for the treatment of schizophrenia, bipolar disorder and adjunctive treatment of major depressive disorder.

New Indication Approved: May 6, 2008


Abilify (aripiprazole)

Date of Approval: November 15, 2002

Abilify (aripiprazole) is a psychotropic drug indicated for the treatment of schizophrenia, bipolar disorder and adjunctive treatment of major depressive disorder.

New Indication Approved: May 6, 2008


Vyvanse (lisdexamfetamine dimesylate)

Date of Approval: February 23, 2007

Vyvanse is an amphetamine derivative prodrug administered once-daily for the treatment of Attention Deficit Hyperactivity Disorder. Vyvanse was developed to lower abuse potential by remaining therapeutically inactive until metabolized in the body.

Patient Population Altered: April 23, 2008


Aloxi (palonosetron)

Date of Approval: July 25, 2003

Aloxi is a 5-HT3 receptor antagonist indicated for the prevention of nausea and vomiting associated with chemotherapy.

New Indication Approved: February 29, 2008


Nexium (esomeprazole)

Date of Approval: February 20, 2001

Nexium (esomeprazole magnesium) is a proton pump inhibitor indicated for the healing and maintenance of healing of erosive esophagitis, treatment of heartburn and other symptoms associated with gastroesophageal reflux disease (GERD), for use in combination with amoxicillin and clarithromycin for H. pylori eradication to reduce the risk of duodenal ulcer recurrence, prevention of NSAID-induced gastric ulcers and Zollinger-Ellison Syndrome.

New Dosage Form Approved: February 27, 2008


Abilify (aripiprazole)

Date of Approval: November 15, 2002

Abilify (aripiprazole) is a psychotropic drug indicated for the treatment of schizophrenia, bipolar disorder and adjunctive treatment of major depressive disorder.

Patient Population Altered: February 27, 2008


Avastin (bevacizumab)

Date of Approval: February 26, 2004

Avastin is a recombinant humanized monoclonal IgG1 antibody for the treatment of metastatic colorectal cancer, non-small cell lung cancer and HER2-negative breast cancer.

New Indication Approved: February 22, 2008


Humira (adalimumab)

Date of Approval: December 31, 2002

Humira is a recombinant human IgGl monoclonal antibody specific for human tumor necrosis factor (TNF) indicated for the treatment of rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, Crohn's disease, psoriasis and juvenile idiopathic arthritis.

New Indication Approved: February 21, 2008


Asmanex (mometasone furoate)

Date of Approval: March 30, 2005

Asmanex Twisthaler (mometasone furoate) is an inhaled corticosteroid for the treatment of asthma.

Patient Population Altered: February 4, 2008


Xyzal (levocetirizine dihydrochloride)

Date of Approval: May 25, 2007

Xyzal is an antihistamine for the relief of symptoms associated with allergic rhinitis and urticaria.

New Dosage Form Approved: January 28, 2008


Humira (adalimumab)

Date of Approval: December 31, 2002

Humira is a recombinant human IgGl monoclonal antibody specific for human tumor necrosis factor (TNF) indicated for the treatment of rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, Crohn's disease, psoriasis and juvenile idiopathic arthritis.

New Indication Approved: January 18, 2008


Tysabri (natalizumab)

Date of Approval: November 23, 2004

Tysabri (natalizumab) is a recombinant humanized IgG4κ monoclonal antibody for the treatment of multiple sclerosis and Crohn's disease.

New Indication Approved: January 14, 2008


Cialis (tadalafil)

Date of Approval: November 21, 2003

Cialis is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5) indicated for the treatment of erectile dysfunction. Although there are other drugs on the market for this indication, this drug is different in that it may work up to 36 hours after dosing.

New Dosage Regimen: January 7, 2008


See also: New Drug Approvals, New Drug Applications, Recent Additions to Drugs.com

New Indications and Dosage forms Archive

2008: Jan | Feb | Mar | Apr | May | Jun | Jul | Aug | Sep | Oct | Nov
2007: Jan | Feb | Mar | Apr | May | Jun | Aug | Sep | Oct | Nov | Dec
2006: May | Jul | Oct
2005: Mar | Oct
2004: Jan | Apr | Sep | Nov
2003: Oct

MedNotes
Advertisement