Moexipril Hydrochloride 00093-0017
Product NDC
00093-0017- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 8, 2003
- Listing Expires
- December 31, 2026
- Application
- ANDA076204
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Moexipril Hydrochloride | 7.5 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]
Packaging Options(1)
100 TABLET, FILM COATED in 1 BOTTLE (0093-0017-01)