Dicyclomine Hydrochloride

Product NDC

70518-0858

11-digit product format

705180858

Labeler code

70518

Product ID

70518-0858_8e4e351f-631c-71cd-e053-2a95a90a6160

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

dicyclomine hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA040317

Marketing category

ANDA

Marketing start

2017-11-20

Marketing end

0000-00-00

Substance

DICYCLOMINE HYDROCHLORIDE

Active strength

20 mg/1

Pharmacologic classes

Anticholinergic [EPC],Cholinergic Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record