Details for New Drug Application (NDA): 079072
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NDA 079072 describes GEMFIBROZIL, which is a drug marketed by Natco, Purepac Pharm, Apotex, Ascent Pharms Inc, Aurobindo Pharma Ltd, Cadila, Cadila Pharms Ltd, Caribe Holdings, Chartwell Molecules, Chartwell Rx, Hikma Pharms, Impax Pharms, Invagen Pharms, Northstar Hlthcare, Norvium Bioscience, Sun Pharm Inds Inc, Teva, and Watson Labs, and is included in twenty NDAs. It is available from thirty-three suppliers. Additional details are available on the GEMFIBROZIL profile page.
The generic ingredient in GEMFIBROZIL is gemfibrozil. Thirty-four suppliers are listed for this compound. Additional details are available on the gemfibrozil profile page.
The generic ingredient in GEMFIBROZIL is gemfibrozil. Thirty-four suppliers are listed for this compound. Additional details are available on the gemfibrozil profile page.
Summary for 079072
| Tradename: | GEMFIBROZIL |
| Applicant: | Northstar Hlthcare |
| Ingredient: | gemfibrozil |
| Patents: | 0 |
Pharmacology for NDA: 079072
| Mechanism of Action | Peroxisome Proliferator-activated Receptor alpha Agonists |
Medical Subject Heading (MeSH) Categories for 079072
Suppliers and Packaging for NDA: 079072
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| GEMFIBROZIL | gemfibrozil | TABLET;ORAL | 079072 | ANDA | Northstar RxLLC | 16714-101 | 16714-101-02 | 60 TABLET in 1 BOTTLE (16714-101-02) |
| GEMFIBROZIL | gemfibrozil | TABLET;ORAL | 079072 | ANDA | Northstar RxLLC | 16714-101 | 16714-101-05 | 500 TABLET in 1 BOTTLE (16714-101-05) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 600MG | ||||
| Approval Date: | Sep 13, 2010 | TE: | AB | RLD: | No | ||||
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