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Glycopyrrolate - 13107-014-11 - (Glycopyrrolate)

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Drug Information of Glycopyrrolate

Product NDC: 13107-014
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: 13107-014
Labeler Name: Aurolife Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202675
Marketing Category: ANDA
Start Marketing Date: 20130415

Package Information of Glycopyrrolate

Package NDC: 13107-014-11
Package Description: 10 TABLET in 1 BOTTLE (13107-014-11)

NDC Information of Glycopyrrolate

NDC Code 13107-014-11
Proprietary Name Glycopyrrolate
Package Description 10 TABLET in 1 BOTTLE (13107-014-11)
Product NDC 13107-014
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glycopyrrolate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130415
Marketing Category Name ANDA
Labeler Name Aurolife Pharma, LLC
Substance Name GLYCOPYRROLATE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Glycopyrrolate


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