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Glycopyrrolate - 55111-649-01 - (Glycopyrrolate)

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Drug Information of Glycopyrrolate

Product NDC: 55111-649
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: 55111-649
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040847
Marketing Category: ANDA
Start Marketing Date: 20080714

Package Information of Glycopyrrolate

Package NDC: 55111-649-01
Package Description: 100 TABLET in 1 BOTTLE (55111-649-01)

NDC Information of Glycopyrrolate

NDC Code 55111-649-01
Proprietary Name Glycopyrrolate
Package Description 100 TABLET in 1 BOTTLE (55111-649-01)
Product NDC 55111-649
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glycopyrrolate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080714
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name GLYCOPYRROLATE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Glycopyrrolate


General Information