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Dicyclomine Hydrochloride - 0615-7754-39 - (Dicyclomine Hydrochloride)

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Drug Information of Dicyclomine Hydrochloride

Product NDC: 0615-7754
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: 0615-7754
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085082
Marketing Category: ANDA
Start Marketing Date: 19860619

Package Information of Dicyclomine Hydrochloride

Package NDC: 0615-7754-39
Package Description: 30 CAPSULE in 1 BLISTER PACK (0615-7754-39)

NDC Information of Dicyclomine Hydrochloride

NDC Code 0615-7754-39
Proprietary Name Dicyclomine Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (0615-7754-39)
Product NDC 0615-7754
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dicyclomine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19860619
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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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