NIFEDIPINE - 16590-319-20 - (NIFEDIPINE)

Alphabetical Index


Drug Information of NIFEDIPINE

Product NDC: 16590-319
Proprietary Name: NIFEDIPINE
Non Proprietary Name: NIFEDIPINE
Active Ingredient(s): 10    mg/1 & nbsp;   NIFEDIPINE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of NIFEDIPINE

Product NDC: 16590-319
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072579
Marketing Category: ANDA
Start Marketing Date: 19890428

Package Information of NIFEDIPINE

Package NDC: 16590-319-20
Package Description: 20 CAPSULE, LIQUID FILLED in 1 BOTTLE (16590-319-20)

NDC Information of NIFEDIPINE

NDC Code 16590-319-20
Proprietary Name NIFEDIPINE
Package Description 20 CAPSULE, LIQUID FILLED in 1 BOTTLE (16590-319-20)
Product NDC 16590-319
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NIFEDIPINE
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 19890428
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name NIFEDIPINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of NIFEDIPINE


General Information