SudoGest - 0904-5803-15 - (Pseudoephedrine Hydrochloride)

Alphabetical Index


Drug Information of SudoGest

Product NDC: 0904-5803
Proprietary Name: SudoGest
Non Proprietary Name: Pseudoephedrine Hydrochloride
Active Ingredient(s): 120    mg/1 & nbsp;   Pseudoephedrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of SudoGest

Product NDC: 0904-5803
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077442
Marketing Category: ANDA
Start Marketing Date: 20060428

Package Information of SudoGest

Package NDC: 0904-5803-15
Package Description: 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0904-5803-15)

NDC Information of SudoGest

NDC Code 0904-5803-15
Proprietary Name SudoGest
Package Description 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0904-5803-15)
Product NDC 0904-5803
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pseudoephedrine Hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060428
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of SudoGest


General Information