Home > National Drug Code (NDC) > Dicyclomine Hydrochloride

Dicyclomine Hydrochloride - 24236-385-03 - (dicyclomine hydrochloride)

Alphabetical Index


Drug Information of Dicyclomine Hydrochloride

Product NDC: 24236-385
Proprietary Name: Dicyclomine Hydrochloride
Non Proprietary Name: dicyclomine hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   dicyclomine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dicyclomine Hydrochloride

Product NDC: 24236-385
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040317
Marketing Category: ANDA
Start Marketing Date: 20130213

Package Information of Dicyclomine Hydrochloride

Package NDC: 24236-385-03
Package Description: 20 TABLET in 1 VIAL (24236-385-03)

NDC Information of Dicyclomine Hydrochloride

NDC Code 24236-385-03
Proprietary Name Dicyclomine Hydrochloride
Package Description 20 TABLET in 1 VIAL (24236-385-03)
Product NDC 24236-385
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dicyclomine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130213
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name DICYCLOMINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Dicyclomine Hydrochloride


General Information