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Dicyclomine - 21695-218-60 - (Dicyclomine)

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Drug Information of Dicyclomine

Product NDC: 21695-218
Proprietary Name: Dicyclomine
Non Proprietary Name: Dicyclomine
Active Ingredient(s): 10    mg/1 & nbsp;   Dicyclomine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Dicyclomine

Product NDC: 21695-218
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040204
Marketing Category: ANDA
Start Marketing Date: 19970228

Package Information of Dicyclomine

Package NDC: 21695-218-60
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC (21695-218-60)

NDC Information of Dicyclomine

NDC Code 21695-218-60
Proprietary Name Dicyclomine
Package Description 60 CAPSULE in 1 BOTTLE, PLASTIC (21695-218-60)
Product NDC 21695-218
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dicyclomine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19970228
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
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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