Nifedipine 68382-0687
Product NDC
68382-0687- Manufacturer
- Zydus Pharmaceuticals (usa) Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 2, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA210012
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Nifedipine | 90 mg/1 |
Drug Class
Dihydropyridine Calcium Channel Blocker [EPC]Calcium Channel Antagonists [MoA]Dihydropyridine Calcium Channel Blocker [EPC]
Packaging Options(3)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-687-01)
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-687-10)
300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-687-95)