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Glycopyrrolate - 0603-3181-10 - (glycopyrrolate)

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Drug Information of Glycopyrrolate

Product NDC: 0603-3181
Proprietary Name: Glycopyrrolate
Non Proprietary Name: glycopyrrolate
Active Ingredient(s): 2    mg/1 & nbsp;   glycopyrrolate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glycopyrrolate

Product NDC: 0603-3181
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040821
Marketing Category: ANDA
Start Marketing Date: 20081229

Package Information of Glycopyrrolate

Package NDC: 0603-3181-10
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC (0603-3181-10)

NDC Information of Glycopyrrolate

NDC Code 0603-3181-10
Proprietary Name Glycopyrrolate
Package Description 10 TABLET in 1 BOTTLE, PLASTIC (0603-3181-10)
Product NDC 0603-3181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name glycopyrrolate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081229
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name GLYCOPYRROLATE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Glycopyrrolate


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