BENZTROPINE MESYLATE

Product NDC

70518-0578

11-digit product format

705180578

Labeler code

70518

Product ID

70518-0578_a509751e-de61-5408-e053-2995a90a9f89

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

BENZTROPINE MESYLATE

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA090168

Marketing category

ANDA

Marketing start

2017-06-19

Marketing end

0000-00-00

Substance

BENZTROPINE MESYLATE

Active strength

1 mg/1

Pharmacologic classes

Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record