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Dicyclomine - 55289-095-60 - (Dicyclomine Hydrochloride)

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Drug Information of Dicyclomine

Product NDC: 55289-095
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: 55289-095
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040161
Marketing Category: ANDA
Start Marketing Date: 19961001

Package Information of Dicyclomine

Package NDC: 55289-095-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (55289-095-60)

NDC Information of Dicyclomine

NDC Code 55289-095-60
Proprietary Name Dicyclomine
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (55289-095-60)
Product NDC 55289-095
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 PD-Rx Pharmaceuticals, Inc.
Substance Name DICYCLOMINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Dicyclomine


General Information