Urecholine

Product NDC

51285-697

11-digit product format

512850697

Labeler code

51285

Product ID

51285-697_e304c581-5e5e-44d0-8cec-0bcc0e3d8a9b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bethanechol Chloride

Dosage form

TABLET

Route

ORAL

Labeler

Teva Women's Health, Inc.

Application

ANDA089095

Marketing category

ANDA

Marketing start

2001-02-01

Marketing end

0000-00-00

Substance

BETHANECHOL CHLORIDE

Active strength

5 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record