NDC 71335-2132 – Nifedipine
Nifedipine 90 mg/1 · Tablet, Extended Release · Oral
Product NDC71335-2132
Product details
- Brand name
- Nifedipine
- Generic name
- Nifedipine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210614
- Marketed since
- March 12, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Dihydropyridine Calcium Channel Blocker
Active ingredients
- Nifedipine 90 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2132-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-1) | Jul 27, 2022 |
| 71335-2132-2 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-2) | Jul 27, 2022 |
| 71335-2132-3 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-3) | Jul 27, 2022 |
| 71335-2132-4 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-4) | Jul 27, 2022 |
| 71335-2132-5 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-5) | Jul 27, 2022 |
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