Diltiazem Hydrochloride 00093-0321
Product NDC
00093-0321- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 26, 1995
- Listing Expires
- December 31, 2026
- Application
- ANDA074185
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Diltiazem Hydrochloride | 120 mg/1 |
Drug Class
Calcium Channel Antagonists [MoA]Calcium Channel Blocker [EPC]Cytochrome P450 3A4 Inhibitors [MoA]
Packaging Options(1)
100 TABLET, FILM COATED in 1 BOTTLE (0093-0321-01)