Details for New Drug Application (NDA): 212284
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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 212284
Tradename: | RANOLAZINE |
Applicant: | Mankind Pharma |
Ingredient: | ranolazine |
Patents: | 0 |
Suppliers and Packaging for NDA: 212284
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
RANOLAZINE | ranolazine | TABLET, EXTENDED RELEASE;ORAL | 212284 | ANDA | McKesson Corporation dba SKY Packaging | 63739-229 | 63739-229-01 | 3 BLISTER PACK in 1 CARTON (63739-229-01) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
RANOLAZINE | ranolazine | TABLET, EXTENDED RELEASE;ORAL | 212284 | ANDA | Lifestar Pharma LLC | 70756-703 | 70756-703-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70756-703-60) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 500MG | ||||
Approval Date: | Feb 12, 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 12, 2020 | TE: | AB | RLD: | No |
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