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Dicyclomine Hydrochloride - 0527-1282-10 - (Dicyclomine Hydrochloride)

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Drug Information of Dicyclomine Hydrochloride

Product NDC: 0527-1282
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: 0527-1282
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040230
Marketing Category: ANDA
Start Marketing Date: 19990226

Package Information of Dicyclomine Hydrochloride

Package NDC: 0527-1282-10
Package Description: 1000 TABLET in 1 BOTTLE (0527-1282-10)

NDC Information of Dicyclomine Hydrochloride

NDC Code 0527-1282-10
Proprietary Name Dicyclomine Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (0527-1282-10)
Product NDC 0527-1282
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dicyclomine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990226
Marketing Category Name ANDA
Labeler Name Lannett Company, Inc.
Substance Name DICYCLOMINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Dicyclomine Hydrochloride


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