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Glycopyrrolate - 64376-601-31 - (Glycopyrrolate)

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Drug Information of Glycopyrrolate

Product NDC: 64376-601
Proprietary Name: Glycopyrrolate
Non Proprietary Name: Glycopyrrolate
Active Ingredient(s): 1    mg/1 & nbsp;   Glycopyrrolate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glycopyrrolate

Product NDC: 64376-601
Labeler Name: Boca Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090020
Marketing Category: ANDA
Start Marketing Date: 20111019

Package Information of Glycopyrrolate

Package NDC: 64376-601-31
Package Description: 30 TABLET in 1 BOTTLE (64376-601-31)

NDC Information of Glycopyrrolate

NDC Code 64376-601-31
Proprietary Name Glycopyrrolate
Package Description 30 TABLET in 1 BOTTLE (64376-601-31)
Product NDC 64376-601
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glycopyrrolate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111019
Marketing Category Name ANDA
Labeler Name Boca Pharmacal, Inc.
Substance Name GLYCOPYRROLATE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Glycopyrrolate


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