Benztropine Mesylate

Product NDC

70518-1217

11-digit product format

705181217

Labeler code

70518

Product ID

70518-1217_90af7e21-e5a7-fd4a-e053-2a95a90a435b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benztropine

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA090294

Marketing category

ANDA

Marketing start

2018-05-17

Marketing end

0000-00-00

Substance

BENZTROPINE MESYLATE

Active strength

2 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