Nifedipine
- Product NDC
- 55289-907
- 11-digit product format
- 552890907
- Labeler code
- 55289
- Product ID
- 55289-907_d2942db2-ea00-803c-e053-2995a90a9153
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA072781
- Marketing category
- ANDA
- Marketing start
- 2009-08-11
- Marketing end
- 0000-00-00
- Substance
- NIFEDIPINE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55289-907-08 | 55289090708 | 8 CAPSULE in 1 BOTTLE, PLASTIC (55289-907-08) | 8 capsule | 2016-06-29 | 0000-00-00 | No | No | Current |
| 55289-907-30 | 55289090730 | 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-907-30) | 30 capsule | 2009-08-11 | 0000-00-00 | No | No | Current |
| 55289-907-79 | 55289090779 | 1 CAPSULE in 1 BOTTLE, PLASTIC (55289-907-79) | 1 capsule | 2009-08-11 | 0000-00-00 | No | No | Current |