Amlodipine Besylate 67877-0199
Product NDC
67877-0199- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 20, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA078925
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amlodipine Besylate | 10 mg/1 |
Drug Class
Calcium Channel Antagonists [MoA]Calcium Channel Blocker [EPC]Cytochrome P450 3A Inhibitors [MoA]
Packaging Options(4)
500 TABLET in 1 BOTTLE (67877-199-05)
1000 TABLET in 1 BOTTLE (67877-199-10)
10 BLISTER PACK in 1 CARTON (67877-199-38) / 10 TABLET in 1 BLISTER PACK
90 TABLET in 1 BOTTLE (67877-199-90)