Dicyclomine Hydrochloride

Product NDC

58118-0795

11-digit product format

581180795

Labeler code

58118

Product ID

58118-0795_9092cbf3-0f34-7138-e053-2a95a90a1836

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Dicyclomine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Clinical Solutions Wholesale

Application

ANDA085223

Marketing category

ANDA

Marketing start

1986-07-30

Marketing end

2020-01-01

Substance

DICYCLOMINE HYDROCHLORIDE

Active strength

20 mg/1

Pharmacologic classes

Anticholinergic [EPC],Cholinergic Antagonists [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record