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Last Updated: November 25, 2024

Details for New Drug Application (NDA): 210054


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NDA 210054 describes RANOLAZINE, which is a drug marketed by Accord Hlthcare, Actavis Elizabeth, Ajanta Pharma Ltd, Alkem Labs Ltd, Allied, Amneal, Ani Pharms, Aurobindo Pharma, Cadila, Chartwell Rx, Cipla, Glenmark Pharms Ltd, Hetero Labs Ltd Iii, Mankind Pharma, Micro Labs, Novast Labs, Piramal, Praxgen, Rising, Sciegen Pharms Inc, Sun Pharm, Sunshine, Unichem, and Vkt Pharma, and is included in twenty-four NDAs. It is available from twenty-seven suppliers. Additional details are available on the RANOLAZINE profile page.

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 210054
Tradename:RANOLAZINE
Applicant:Ajanta Pharma Ltd
Ingredient:ranolazine
Patents:0
Suppliers and Packaging for NDA: 210054
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
RANOLAZINE ranolazine TABLET, EXTENDED RELEASE;ORAL 210054 ANDA Ajanta Pharma USA Inc. 27241-125 27241-125-02 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-125-02)
RANOLAZINE ranolazine TABLET, EXTENDED RELEASE;ORAL 210054 ANDA Ajanta Pharma USA Inc. 27241-125 27241-125-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-125-05)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength500MG
Approval Date:May 28, 2019TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength1GM
Approval Date:May 28, 2019TE:ABRLD:No

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