Nifedipine 70771-1365
Product NDC
70771-1365- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 18, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA210184
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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(6)
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-0)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-1)
10 BLISTER PACK in 1 CARTON (70771-1365-4) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-5)
300 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-7)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-9)