Nifedipine 68682-0108
Product NDC
68682-0108- Manufacturer
- Oceanside Pharmaceuticals
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 27, 2000
- Listing Expires
- December 31, 2027
- Application
- ANDA075289
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Nifedipine | 30 mg/1 |
Drug Class
Dihydropyridine Calcium Channel Blocker [EPC]Calcium Channel Antagonists [MoA]Dihydropyridine Calcium Channel Blocker [EPC]
Packaging Options(2)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-108-10)
300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-108-30)