Details for New Drug Application (NDA): 214035
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The generic ingredient in RANOLAZINE is ranolazine. There are twenty-three drug master file entries for this compound. Twenty-seven suppliers are listed for this compound. Additional details are available on the ranolazine profile page.
Summary for 214035
| Tradename: | RANOLAZINE |
| Applicant: | Vkt Pharma |
| Ingredient: | ranolazine |
| Patents: | 0 |
Suppliers and Packaging for NDA: 214035
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| RANOLAZINE | ranolazine | TABLET, EXTENDED RELEASE;ORAL | 214035 | ANDA | Torrent Pharma, Inc. | 13668-759 | 13668-759-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (13668-759-60) |
| RANOLAZINE | ranolazine | TABLET, EXTENDED RELEASE;ORAL | 214035 | ANDA | Torrent Pharma, Inc. | 13668-760 | 13668-760-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (13668-760-60) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 500MG | ||||
| Approval Date: | Jan 19, 2022 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 1GM | ||||
| Approval Date: | Jan 19, 2022 | TE: | AB | RLD: | No | ||||
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