Ranolazine 63304-0018
Product NDC
63304-0018- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 28, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA211707
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ranolazine | 1000 mg/1 |
Drug Class
Anti-anginal [EPC]Anti-anginal [EPC]Cytochrome P450 2D6 Inhibitors [MoA]
Packaging Options(3)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-05)
180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-28)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-60)