Moexipril Hydrochloride 68462-0208
Product NDC
68462-0208- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 31, 2010
- Listing Expires
- December 31, 2027
- Application
- ANDA090416
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Moexipril Hydrochloride | 15 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (68462-208-01)
1000 TABLET, FILM COATED in 1 BOTTLE (68462-208-10)
90 TABLET, FILM COATED in 1 BOTTLE (68462-208-90)