NDC 68084-603 – Nifedipine
Nifedipine 90 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68084-603
Product details
- Brand name
- Nifedipine
- Generic name
- Nifedipine
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077127
- Marketed since
- August 21, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Dihydropyridine Calcium Channel Blocker
Active ingredients
- Nifedipine 90 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68084-603-21 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-603-21) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-603-11) | Aug 21, 2012 |
| 68084-603-65 | 50 BLISTER PACK in 1 CARTON (68084-603-65) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-603-11) | Feb 6, 2023 |
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