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Glycopyrrolate - 0143-9682-25 - (Glycopyrrolate)

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Drug Information of Glycopyrrolate

Product NDC: 0143-9682
Proprietary Name: Glycopyrrolate
Non Proprietary Name: Glycopyrrolate
Active Ingredient(s): .2    mg/mL & nbsp;   Glycopyrrolate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Glycopyrrolate

Product NDC: 0143-9682
Labeler Name: West-Ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090963
Marketing Category: ANDA
Start Marketing Date: 20110921

Package Information of Glycopyrrolate

Package NDC: 0143-9682-25
Package Description: 25 VIAL in 1 CARTON (0143-9682-25) > 1 mL in 1 VIAL (0143-9682-01)

NDC Information of Glycopyrrolate

NDC Code 0143-9682-25
Proprietary Name Glycopyrrolate
Package Description 25 VIAL in 1 CARTON (0143-9682-25) > 1 mL in 1 VIAL (0143-9682-01)
Product NDC 0143-9682
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glycopyrrolate
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110921
Marketing Category Name ANDA
Labeler Name West-Ward Pharmaceutical Corp
Substance Name GLYCOPYRROLATE
Strength Number .2
Strength Unit mg/mL
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Glycopyrrolate


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