Nifedipine
- Product NDC
- 50090-2917
- 11-digit product format
- 500902917
- Labeler code
- 50090
- Product ID
- 50090-2917_a5fc4989-4a95-45f9-903c-66b477f24d5f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nifedipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA201071
- Marketing category
- ANDA
- Marketing start
- 2010-12-20
- Marketing end
- 0000-00-00
- Substance
- NIFEDIPINE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Calcium Channel
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record