Ranolazine 68462-0319
Product NDC
68462-0319- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 5, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA211082
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ranolazine | 500 mg/1 |
Drug Class
Anti-anginal [EPC]Anti-anginal [EPC]Cytochrome P450 2D6 Inhibitors [MoA]
Packaging Options(2)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-319-05)
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-319-60)