Details for New Drug Application (NDA): 210184
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NDA 210184 describes NIFEDIPINE, which is a drug marketed by Acella, Actavis Elizabeth, Chase Labs Nj, Heritage Pharma, Teva, Velzen Pharma Pvt, Alembic, Alkem Labs Ltd, Aurobindo Pharma, Aurobindo Pharma Usa, Elite Pharm Solution, Endo Operations, Martec Usa Llc, Norvium Bioscience, Novast Labs, Osmotica Pharm Us, Rising, Spil, Swiss Pharm, Twi Pharms, Valeant Pharms North, and Zydus Pharms, and is included in thirty NDAs. It is available from thirty-six suppliers. Additional details are available on the NIFEDIPINE profile page.
The generic ingredient in NIFEDIPINE is nifedipine. There are thirty-nine drug master file entries for this compound. Thirty-eight suppliers are listed for this compound. Additional details are available on the nifedipine profile page.
The generic ingredient in NIFEDIPINE is nifedipine. There are thirty-nine drug master file entries for this compound. Thirty-eight suppliers are listed for this compound. Additional details are available on the nifedipine profile page.
Summary for 210184
| Tradename: | NIFEDIPINE |
| Applicant: | Zydus Pharms |
| Ingredient: | nifedipine |
| Patents: | 0 |
Pharmacology for NDA: 210184
| Mechanism of Action | Calcium Channel Antagonists |
Medical Subject Heading (MeSH) Categories for 210184
Suppliers and Packaging for NDA: 210184
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| NIFEDIPINE | nifedipine | TABLET, EXTENDED RELEASE;ORAL | 210184 | ANDA | Zydus Pharmaceuticals (USA) Inc. | 68382-688 | 68382-688-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-01) |
| NIFEDIPINE | nifedipine | TABLET, EXTENDED RELEASE;ORAL | 210184 | ANDA | Zydus Pharmaceuticals (USA) Inc. | 68382-688 | 68382-688-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-05) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 30MG | ||||
| Approval Date: | Jun 29, 2018 | TE: | AB1 | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 60MG | ||||
| Approval Date: | Jun 29, 2018 | TE: | AB1 | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 90MG | ||||
| Approval Date: | Jun 29, 2018 | TE: | AB1 | RLD: | No | ||||
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