NDC 71335-1721 – Nifedipine
Nifedipine 60 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71335-1721
Product details
- Brand name
- Nifedipine
- Generic name
- nifedipine
- Labeler
- Bryant Ranch Prepack
- 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 60 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1721-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1721-1) | Oct 20, 2020 |
| 71335-1721-2 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1721-2) | Oct 20, 2020 |
| 71335-1721-3 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1721-3) | Oct 20, 2020 |
| 71335-1721-4 | 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1721-4) | Oct 20, 2020 |
| 71335-1721-5 | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1721-5) | Oct 20, 2020 |
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