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Dicyclomine Hydrochloride - 49999-081-20 - (Dicyclomine Hydrochloride)

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Drug Information of Dicyclomine Hydrochloride

Product NDC: 49999-081
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: 49999-081
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085223
Marketing Category: ANDA
Start Marketing Date: 20111118

Package Information of Dicyclomine Hydrochloride

Package NDC: 49999-081-20
Package Description: 20 TABLET in 1 BOTTLE (49999-081-20)

NDC Information of Dicyclomine Hydrochloride

NDC Code 49999-081-20
Proprietary Name Dicyclomine Hydrochloride
Package Description 20 TABLET in 1 BOTTLE (49999-081-20)
Product NDC 49999-081
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dicyclomine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111118
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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