Product NDC: | 41520-054 |
Proprietary Name: | careone suphedrine 12 hour relief |
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) |
Product NDC: | 41520-054 |
Labeler Name: | American Sales Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075153 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040511 |
Package NDC: | 41520-054-52 |
Package Description: | 1 BLISTER PACK in 1 CARTON (41520-054-52) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Code | 41520-054-52 |
Proprietary Name | careone suphedrine 12 hour relief |
Package Description | 1 BLISTER PACK in 1 CARTON (41520-054-52) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 41520-054 |
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 | 20040511 |
Marketing Category Name | ANDA |
Labeler Name | American Sales Company |
Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 120 |
Strength Unit | mg/1 |
Pharmaceutical Classes |