NDC 68682-108 – Nifedipine
Nifedipine 30 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68682-108
Product details
- Brand name
- Nifedipine
- Generic name
- Nifedipine
- Labeler
- Oceanside Pharmaceuticals
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA075289
- Marketed since
- September 27, 2000
- Listing expires
- December 31, 2027
- Pharmacologic class
- Dihydropyridine Calcium Channel Blocker
Active ingredients
- Nifedipine 30 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68682-108-10 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-108-10) | Sep 27, 2000 |
| 68682-108-30 | 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-108-30) | Sep 27, 2000 |
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