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Dicyclomine Hydrochloride - 0378-1620-05 - (dicyclomine hydrochloride)

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Drug Information of Dicyclomine Hydrochloride

Product NDC: 0378-1620
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: 0378-1620
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040317
Marketing Category: ANDA
Start Marketing Date: 20130327

Package Information of Dicyclomine Hydrochloride

Package NDC: 0378-1620-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (0378-1620-05)

NDC Information of Dicyclomine Hydrochloride

NDC Code 0378-1620-05
Proprietary Name Dicyclomine Hydrochloride
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (0378-1620-05)
Product NDC 0378-1620
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dicyclomine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130327
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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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