SudoGest - 63629-1491-4 - (Pseudoephedrine Hydrochloride)

Alphabetical Index


Drug Information of SudoGest

Product NDC: 63629-1491
Proprietary Name: SudoGest
Non Proprietary Name: Pseudoephedrine Hydrochloride
Active Ingredient(s): 60    mg/1 & nbsp;   Pseudoephedrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of SudoGest

Product NDC: 63629-1491
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19941001

Package Information of SudoGest

Package NDC: 63629-1491-4
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (63629-1491-4)

NDC Information of SudoGest

NDC Code 63629-1491-4
Proprietary Name SudoGest
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (63629-1491-4)
Product NDC 63629-1491
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pseudoephedrine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19941001
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Bryant Ranch Prepack
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]

Complete Information of SudoGest


General Information