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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 211745


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NDA 211745 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 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:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength500MG
Approval Date:Feb 27, 2020TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength1GM
Approval Date:Feb 27, 2020TE:ABRLD:No

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