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Glycopyrrolate - 0722-7097-01 - (Glycopyrrolate)

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Drug Information of Glycopyrrolate

Product NDC: 0722-7097
Proprietary Name: Glycopyrrolate
Non Proprietary Name: Glycopyrrolate
Active Ingredient(s): 1.5    mg/1 & nbsp;   Glycopyrrolate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glycopyrrolate

Product NDC: 0722-7097
Labeler Name: Nexgen Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091522
Marketing Category: ANDA
Start Marketing Date: 20120312

Package Information of Glycopyrrolate

Package NDC: 0722-7097-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0722-7097-01)

NDC Information of Glycopyrrolate

NDC Code 0722-7097-01
Proprietary Name Glycopyrrolate
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0722-7097-01)
Product NDC 0722-7097
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glycopyrrolate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120312
Marketing Category Name ANDA
Labeler Name Nexgen Pharma, Inc.
Substance Name GLYCOPYRROLATE
Strength Number 1.5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Glycopyrrolate


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