Procardia
- Product NDC
- 0069-2600
- 11-digit product format
- 000692600
- Labeler code
- 0069
- Product ID
- 0069-2600_4d73954d-2e15-4db3-bbe2-98606f9aac4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nifedipine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Application
- NDA018482
- Marketing category
- NDA
- Marketing start
- 1981-12-31
- Marketing end
- 2021-10-31
- 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
- 0000-00-00
- 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 |
|---|
| 0069-2600-66 | 00069260066 | 100 CAPSULE in 1 BOTTLE (0069-2600-66) | 100 capsule | 1981-12-31 | 2021-10-31 | No | No | Current |