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Dicyclomine - 68788-9934-6 - (Dicyclomine Hydrochloride)

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Drug Information of Dicyclomine

Product NDC: 68788-9934
Proprietary Name: Dicyclomine
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

Product NDC: 68788-9934
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040161
Marketing Category: ANDA
Start Marketing Date: 20120117

Package Information of Dicyclomine

Package NDC: 68788-9934-6
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (68788-9934-6)

NDC Information of Dicyclomine

NDC Code 68788-9934-6
Proprietary Name Dicyclomine
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (68788-9934-6)
Product NDC 68788-9934
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dicyclomine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120117
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name DICYCLOMINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Dicyclomine


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