Details for New Drug Application (NDA): 075753
✉ Email this page to a colleague
NDA 075753 describes FENOFIBRATE (MICRONIZED), which is a drug marketed by Ajanta Pharma Ltd, Alembic, Ani Pharms, Apotex, Aurobindo Pharma Ltd, Chartwell, Dr Reddys Labs Sa, Glenmark Pharms Ltd, Impax Labs, Invagen Pharms, Norvium Bioscience, Novast Labs, Reyoung, Rhodes Pharms, Rising, and Torrent, and is included in sixteen NDAs. It is available from seventeen suppliers. Additional details are available on the FENOFIBRATE (MICRONIZED) profile page.
The generic ingredient in FENOFIBRATE (MICRONIZED) is fenofibrate. There are forty-two drug master file entries for this compound. Fifty-four suppliers are listed for this compound. Additional details are available on the fenofibrate profile page.
The generic ingredient in FENOFIBRATE (MICRONIZED) is fenofibrate. There are forty-two drug master file entries for this compound. Fifty-four suppliers are listed for this compound. Additional details are available on the fenofibrate profile page.
Summary for 075753
| Tradename: | FENOFIBRATE (MICRONIZED) |
| Applicant: | Rhodes Pharms |
| Ingredient: | fenofibrate |
| Patents: | 0 |
Suppliers and Packaging for NDA: 075753
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| FENOFIBRATE (MICRONIZED) | fenofibrate | CAPSULE;ORAL | 075753 | ANDA | Rhodes Pharmaceuticals L.P. | 42858-067 | 42858-067-01 | 100 CAPSULE in 1 BOTTLE (42858-067-01) |
| FENOFIBRATE (MICRONIZED) | fenofibrate | CAPSULE;ORAL | 075753 | ANDA | Rhodes Pharmaceuticals L.P. | 42858-134 | 42858-134-01 | 100 CAPSULE in 1 BOTTLE (42858-134-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 67MG | ||||
| Approval Date: | Sep 3, 2002 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 134MG | ||||
| Approval Date: | Apr 9, 2002 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 200MG | ||||
| Approval Date: | Apr 9, 2002 | TE: | AB | RLD: | No | ||||
Complete Access Available with Subscription
