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Last Updated: November 24, 2024

Details for New Drug Application (NDA): 211354


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NDA 211354 describes AMANTADINE HYDROCHLORIDE, which is a drug marketed by Zydus, Actavis Elizabeth, Alembic, Bionpharma, Chartwell Molecular, Heritage Pharma, Humanwell Puracap, Invagen Pharms, Rising, Rubicon, Sandoz, Strides Pharma, Upsher Smith Labs, Watson Labs, Watson Labs Inc, Zydus Pharms, Aurobindo Pharma Usa, Chartwell Rx, Cmp Pharma Inc, Elysium, Endo Operations, G And W Labs Inc, Pharm Assoc, Teva Pharms, Xttrium Labs Inc, Adaptis, Athem, Jubilant Generics, and Zhejiang Jutai Pharm, and is included in thirty-six NDAs. It is available from thirty-two suppliers. Additional details are available on the AMANTADINE HYDROCHLORIDE profile page.

The generic ingredient in AMANTADINE HYDROCHLORIDE is amantadine hydrochloride. There are seven drug master file entries for this compound. Thirty-three suppliers are listed for this compound. Additional details are available on the amantadine hydrochloride profile page.
Summary for 211354
Tradename:AMANTADINE HYDROCHLORIDE
Applicant:Strides Pharma
Ingredient:amantadine hydrochloride
Patents:0
Pharmacology for NDA: 211354
Mechanism of ActionM2 Protein Inhibitors
Medical Subject Heading (MeSH) Categories for 211354
Suppliers and Packaging for NDA: 211354
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
AMANTADINE HYDROCHLORIDE amantadine hydrochloride CAPSULE;ORAL 211354 ANDA Strides Pharma Science Limited 64380-862 64380-862-06 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (64380-862-06)
AMANTADINE HYDROCHLORIDE amantadine hydrochloride CAPSULE;ORAL 211354 ANDA Strides Pharma Science Limited 64380-862 64380-862-07 500 CAPSULE, LIQUID FILLED in 1 BOTTLE (64380-862-07)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength100MG
Approval Date:Feb 18, 2022TE:ABRLD:No

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