Dicyclomine Hydrochloride

Product NDC

71335-0588

11-digit product format

713350588

Labeler code

71335

Product ID

71335-0588_1a7a5872-3bff-492b-914f-17c8c8e8a8db

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

dicyclomine hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA040319

Marketing category

ANDA

Marketing start

1999-11-03

Marketing end

0000-00-00

Substance

DICYCLOMINE HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

Anticholinergic [EPC],Cholinergic Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record