Trandolapril And Verapamil Hydrochloride 68462-0295
Product NDC
68462-0295- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 25, 2015
- Listing Expires
- December 31, 2027
- Application
- ANDA079135
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Trandolapril | 2 mg/1 |
| Verapamil Hydrochloride | 180 mg/1 |
Drug Class
Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]
Packaging Options(3)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-295-01)
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-295-10)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-295-90)