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Glycopyrrolate - 55154-5739-8 - (Glycopyrrolate)

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Drug Information of Glycopyrrolate

Product NDC: 55154-5739
Proprietary Name: Glycopyrrolate
Non Proprietary Name: Glycopyrrolate
Active Ingredient(s): .4    mg/2mL & nbsp;   Glycopyrrolate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Glycopyrrolate

Product NDC: 55154-5739
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089335
Marketing Category: ANDA
Start Marketing Date: 20111025

Package Information of Glycopyrrolate

Package NDC: 55154-5739-8
Package Description: 1 VIAL, MULTI-DOSE in 1 BAG (55154-5739-8) > 2 mL in 1 VIAL, MULTI-DOSE

NDC Information of Glycopyrrolate

NDC Code 55154-5739-8
Proprietary Name Glycopyrrolate
Package Description 1 VIAL, MULTI-DOSE in 1 BAG (55154-5739-8) > 2 mL in 1 VIAL, MULTI-DOSE
Product NDC 55154-5739
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glycopyrrolate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20111025
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name GLYCOPYRROLATE
Strength Number .4
Strength Unit mg/2mL
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Glycopyrrolate


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