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Robinul Forte - 59630-205-10 - (Glycopyrrolate)

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Drug Information of Robinul Forte

Product NDC: 59630-205
Proprietary Name: Robinul Forte
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 Robinul Forte

Product NDC: 59630-205
Labeler Name: Shionogi Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA012827
Marketing Category: NDA
Start Marketing Date: 19610328

Package Information of Robinul Forte

Package NDC: 59630-205-10
Package Description: 100 TABLET in 1 BOTTLE (59630-205-10)

NDC Information of Robinul Forte

NDC Code 59630-205-10
Proprietary Name Robinul Forte
Package Description 100 TABLET in 1 BOTTLE (59630-205-10)
Product NDC 59630-205
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glycopyrrolate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19610328
Marketing Category Name NDA
Labeler Name Shionogi Inc.
Substance Name GLYCOPYRROLATE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Robinul Forte


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