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DICYCLOMINE HYDROCHLORIDE - 49349-002-02 - (DICYCLOMINE)

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Drug Information of DICYCLOMINE HYDROCHLORIDE

Product NDC: 49349-002
Proprietary Name: DICYCLOMINE HYDROCHLORIDE
Non Proprietary Name: DICYCLOMINE
Active Ingredient(s): 20    mg/1 & nbsp;   DICYCLOMINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of DICYCLOMINE HYDROCHLORIDE

Product NDC: 49349-002
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040161
Marketing Category: ANDA
Start Marketing Date: 20100723

Package Information of DICYCLOMINE HYDROCHLORIDE

Package NDC: 49349-002-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-002-02)

NDC Information of DICYCLOMINE HYDROCHLORIDE

NDC Code 49349-002-02
Proprietary Name DICYCLOMINE HYDROCHLORIDE
Package Description 30 TABLET in 1 BLISTER PACK (49349-002-02)
Product NDC 49349-002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DICYCLOMINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100723
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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