Urecholine

Product NDC

51285-691

11-digit product format

512850691

Labeler code

51285

Product ID

51285-691_c08ddeaf-c772-4e32-92a8-9fb81dc94ddb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bethanechol Chloride

Dosage form

TABLET

Route

ORAL

Labeler

Teva Women's Health, Inc.

Application

ANDA088441

Marketing category

ANDA

Marketing start

2000-04-01

Marketing end

2020-08-31

Substance

BETHANECHOL CHLORIDE

Active strength

25 mg/1

Pharmacologic classes

Cholinergic Muscarinic Agonist [EPC],Cholinergic Muscarinic Agonists [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record