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Dicyclomine Hydrochloride - 49999-291-30 - (Dicyclomine Hydrochloride)

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Drug Information of Dicyclomine Hydrochloride

Product NDC: 49999-291
Proprietary Name: Dicyclomine Hydrochloride
Non Proprietary Name: Dicyclomine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Dicyclomine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Dicyclomine Hydrochloride

Product NDC: 49999-291
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084285
Marketing Category: ANDA
Start Marketing Date: 19740930

Package Information of Dicyclomine Hydrochloride

Package NDC: 49999-291-30
Package Description: 30 CAPSULE in 1 BOTTLE (49999-291-30)

NDC Information of Dicyclomine Hydrochloride

NDC Code 49999-291-30
Proprietary Name Dicyclomine Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE (49999-291-30)
Product NDC 49999-291
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dicyclomine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19740930
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name DICYCLOMINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Dicyclomine Hydrochloride


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