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Dicyclomine Hydrochloride - 54868-0818-4 - (Dicyclomine Hydrochloride)

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Drug Information of Dicyclomine Hydrochloride

Product NDC: 54868-0818
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: 54868-0818
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040161
Marketing Category: ANDA
Start Marketing Date: 19950123

Package Information of Dicyclomine Hydrochloride

Package NDC: 54868-0818-4
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (54868-0818-4)

NDC Information of Dicyclomine Hydrochloride

NDC Code 54868-0818-4
Proprietary Name Dicyclomine Hydrochloride
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (54868-0818-4)
Product NDC 54868-0818
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dicyclomine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950123
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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