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Dicyclomine Hydrochloride - 52125-651-02 - (dicyclomine hydrochloride)

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Drug Information of Dicyclomine Hydrochloride

Product NDC: 52125-651
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: 52125-651
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040319
Marketing Category: ANDA
Start Marketing Date: 20130701

Package Information of Dicyclomine Hydrochloride

Package NDC: 52125-651-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (52125-651-02)

NDC Information of Dicyclomine Hydrochloride

NDC Code 52125-651-02
Proprietary Name Dicyclomine Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (52125-651-02)
Product NDC 52125-651
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dicyclomine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130701
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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