Amantadine Hydrochloride

Product NDC

0832-2012

11-digit product format

008322012

Labeler code

0832

Product ID

0832-2012_dc5841ec-abee-4031-96bb-b9693ab0b211

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amantadine Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Upsher-Smith Laboratories, Inc.

Application

ANDA071293

Marketing category

ANDA

Marketing start

1987-02-18

Marketing end

0000-00-00

Substance

AMANTADINE HYDROCHLORIDE

Active strength

100 mg/1

Pharmacologic classes

Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record