Product NDC: | 52959-260 |
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) |
Product NDC: | 52959-260 |
Labeler Name: | H.J. Harkins Company, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19941001 |
Package NDC: | 52959-260-60 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-260-60) |
NDC Code | 52959-260-60 |
Proprietary Name | SudoGest |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-260-60) |
Product NDC | 52959-260 |
Product Type Name | HUMAN OTC 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 | H.J. Harkins Company, Inc. |
Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 60 |
Strength Unit | mg/1 |
Pharmaceutical Classes |