SudoGest - 21695-806-12 - (Pseudoephedrine Hydrochloride)

Alphabetical Index


Drug Information of SudoGest

Product NDC: 21695-806
Proprietary Name: SudoGest
Non Proprietary Name: Pseudoephedrine Hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   Pseudoephedrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of SudoGest

Product NDC: 21695-806
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19941001

Package Information of SudoGest

Package NDC: 21695-806-12
Package Description: 12 TABLET in 1 BLISTER PACK (21695-806-12)

NDC Information of SudoGest

NDC Code 21695-806-12
Proprietary Name SudoGest
Package Description 12 TABLET in 1 BLISTER PACK (21695-806-12)
Product NDC 21695-806
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pseudoephedrine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19941001
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rebel Distributors Corp
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of SudoGest


General Information