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 | Laurus Generics Inc. | 42385-963 | 42385-963-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42385-963-60) |
RANOLAZINE | ranolazine | TABLET, EXTENDED RELEASE;ORAL | 214035 | ANDA | Laurus Generics Inc. | 42385-964 | 42385-964-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42385-964-60) |
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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