Details for New Drug Application (NDA): 208096

NDA 208096 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 208096

Tradename:	AMANTADINE HYDROCHLORIDE
Applicant:	Watson Labs Inc
Ingredient:	amantadine hydrochloride
Patents:	0

Pharmacology for NDA: 208096

Mechanism of Action

M2 Protein Inhibitors

Medical Subject Heading (MeSH) Categories for 208096

Analgesics, Non-Narcotic

Antiparkinson Agents

Antiviral Agents

Dopamine Agents

Suppliers and Packaging for NDA: 208096

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
AMANTADINE HYDROCHLORIDE	amantadine hydrochloride	TABLET;ORAL	208096	ANDA	Actavis Pharma, Inc.	0591-4920	0591-4920-01	100 TABLET in 1 BOTTLE (0591-4920-01)
AMANTADINE HYDROCHLORIDE	amantadine hydrochloride	TABLET;ORAL	208096	ANDA	Actavis Pharma, Inc.	0591-4920	0591-4920-05	500 TABLET in 1 BOTTLE (0591-4920-05)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	100MG
Approval Date:	Dec 15, 2016	TE:	AB	RLD:	No

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