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Glycopyrrolate - 52584-009-36 - (Glycopyrrolate)

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Drug Information of Glycopyrrolate

Product NDC: 52584-009
Proprietary Name: Glycopyrrolate
Non Proprietary Name: Glycopyrrolate
Active Ingredient(s): .2    mg/mL & nbsp;   Glycopyrrolate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Glycopyrrolate

Product NDC: 52584-009
Labeler Name: General Injectables & Vaccines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017558
Marketing Category: NDA
Start Marketing Date: 20100301

Package Information of Glycopyrrolate

Package NDC: 52584-009-36
Package Description: 1 VIAL, MULTI-DOSE in 1 BAG (52584-009-36) > 5 mL in 1 VIAL, MULTI-DOSE

NDC Information of Glycopyrrolate

NDC Code 52584-009-36
Proprietary Name Glycopyrrolate
Package Description 1 VIAL, MULTI-DOSE in 1 BAG (52584-009-36) > 5 mL in 1 VIAL, MULTI-DOSE
Product NDC 52584-009
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glycopyrrolate
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100301
Marketing Category Name NDA
Labeler Name General Injectables & Vaccines, Inc
Substance Name GLYCOPYRROLATE
Strength Number .2
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Glycopyrrolate


General Information