Details for New Drug Application (NDA): 211745
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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 211745
| Tradename: | RANOLAZINE |
| Applicant: | Micro Labs |
| Ingredient: | ranolazine |
| Patents: | 0 |
Suppliers and Packaging for NDA: 211745
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| RANOLAZINE | ranolazine | TABLET, EXTENDED RELEASE;ORAL | 211745 | ANDA | Micro Labs Limited | 42571-324 | 42571-324-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42571-324-05) |
| RANOLAZINE | ranolazine | TABLET, EXTENDED RELEASE;ORAL | 211745 | ANDA | Micro Labs Limited | 42571-324 | 42571-324-11 | 100 BLISTER PACK in 1 CARTON (42571-324-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (42571-324-32) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 500MG | ||||
| Approval Date: | Feb 27, 2020 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 1GM | ||||
| Approval Date: | Feb 27, 2020 | TE: | AB | RLD: | No | ||||
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