NDC 0904-7082 – Nifedipine
Nifedipine 90 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC0904-7082
Product details
- Brand name
- Nifedipine
- Generic name
- Nifedipine
- Labeler
- Major Pharmaceuticals
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210614
- Marketed since
- March 12, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Dihydropyridine Calcium Channel Blocker
Active ingredients
- Nifedipine 90 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0904-7082-04 | 30 BLISTER PACK in 1 CARTON (0904-7082-04) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Mar 12, 2019 |
| 0904-7082-06 | 50 BLISTER PACK in 1 CARTON (0904-7082-06) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Mar 12, 2019 |
Recalls mentioning this NDC
- D-0652-2021 Jul 21, 2021 · Class II
Failed Dissolution Specification: Out of specification for dissolution during routine stability testing.
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