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Glycopyrrolate - 0517-4605-25 - (Glycopyrrolate)

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Drug Information of Glycopyrrolate

Product NDC: 0517-4605
Proprietary Name: Glycopyrrolate
Non Proprietary Name: Glycopyrrolate
Active Ingredient(s): .2    mg/mL & nbsp;   Glycopyrrolate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Glycopyrrolate

Product NDC: 0517-4605
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089335
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Glycopyrrolate

Package NDC: 0517-4605-25
Package Description: 25 VIAL, MULTI-DOSE in 1 TRAY (0517-4605-25) > 5 mL in 1 VIAL, MULTI-DOSE

NDC Information of Glycopyrrolate

NDC Code 0517-4605-25
Proprietary Name Glycopyrrolate
Package Description 25 VIAL, MULTI-DOSE in 1 TRAY (0517-4605-25) > 5 mL in 1 VIAL, MULTI-DOSE
Product NDC 0517-4605
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glycopyrrolate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name American Regent, Inc.
Substance Name GLYCOPYRROLATE
Strength Number .2
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Glycopyrrolate


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