Benztropine Mesylate

Product NDC

70518-1056

11-digit product format

705181056

Labeler code

70518

Product ID

70518-1056_900e4aaa-fd54-b37d-e053-2995a90a0447

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benztropine

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA090294

Marketing category

ANDA

Marketing start

2018-03-12

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

2020-12-31

Current FDA listing

Historical FDA.report record