Urecholine

Product NDC

51285-690

11-digit product format

512850690

Labeler code

51285

Product ID

51285-690_a17b096f-f970-4d6b-9f8f-19e792406f3d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bethanechol Chloride

Dosage form

TABLET

Route

ORAL

Labeler

Teva Women's Health, Inc.

Application

ANDA088440

Marketing category

ANDA

Marketing start

2001-02-01

Marketing end

2020-02-29

Substance

BETHANECHOL CHLORIDE

Active strength

10 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