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Dicyclomine - 52959-221-30 - (Dicyclomine Hydrochloride)

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Drug Information of Dicyclomine

Product NDC: 52959-221
Proprietary Name: Dicyclomine
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

Product NDC: 52959-221
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040161
Marketing Category: ANDA
Start Marketing Date: 19961001

Package Information of Dicyclomine

Package NDC: 52959-221-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (52959-221-30)

NDC Information of Dicyclomine

NDC Code 52959-221-30
Proprietary Name Dicyclomine
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (52959-221-30)
Product NDC 52959-221
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dicyclomine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19961001
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name DICYCLOMINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Dicyclomine


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