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GLYCOPYRROLATE - 64720-156-01 - (GLYCOPYRROLATE)

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Drug Information of GLYCOPYRROLATE

Product NDC: 64720-156
Proprietary Name: GLYCOPYRROLATE
Non Proprietary Name: GLYCOPYRROLATE
Active Ingredient(s): 2    mg/1 & nbsp;   GLYCOPYRROLATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of GLYCOPYRROLATE

Product NDC: 64720-156
Labeler Name: CorePharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040568
Marketing Category: ANDA
Start Marketing Date: 20041230

Package Information of GLYCOPYRROLATE

Package NDC: 64720-156-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (64720-156-01)

NDC Information of GLYCOPYRROLATE

NDC Code 64720-156-01
Proprietary Name GLYCOPYRROLATE
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (64720-156-01)
Product NDC 64720-156
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GLYCOPYRROLATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041230
Marketing Category Name ANDA
Labeler Name CorePharma, LLC
Substance Name GLYCOPYRROLATE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of GLYCOPYRROLATE


General Information