Amlodipine Besylate 68382-0122
Product NDC
68382-0122- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 21, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA078226
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amlodipine Besylate | 5 mg/1 |
Drug Class
Calcium Channel Antagonists [MoA]Calcium Channel Blocker [EPC]Cytochrome P450 3A Inhibitors [MoA]
Packaging Options(4)
100 TABLET in 1 BOTTLE (68382-122-01)
500 TABLET in 1 BOTTLE (68382-122-05)
90 TABLET in 1 BOTTLE (68382-122-16)
10 BLISTER PACK in 1 CARTON (68382-122-77) / 10 TABLET in 1 BLISTER PACK