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Dicyclomine - 0615-0327-39 - (dicyclomine hydrochloride)

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Drug Information of Dicyclomine

Product NDC: 0615-0327
Proprietary Name: Dicyclomine
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

Product NDC: 0615-0327
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040204
Marketing Category: ANDA
Start Marketing Date: 19970228

Package Information of Dicyclomine

Package NDC: 0615-0327-39
Package Description: 30 CAPSULE in 1 BLISTER PACK (0615-0327-39)

NDC Information of Dicyclomine

NDC Code 0615-0327-39
Proprietary Name Dicyclomine
Package Description 30 CAPSULE in 1 BLISTER PACK (0615-0327-39)
Product NDC 0615-0327
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dicyclomine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19970228
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


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