Product NDC: | 59779-574 |
Proprietary Name: | Severe Sinus Congestion |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 325; 200; 30 mg/1; mg/1; mg/1 & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-574 |
Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20080609 |
Package NDC: | 59779-574-08 |
Package Description: | 1 BLISTER PACK in 1 CARTON (59779-574-08) > 24 TABLET in 1 BLISTER PACK |
NDC Code | 59779-574-08 |
Proprietary Name | Severe Sinus Congestion |
Package Description | 1 BLISTER PACK in 1 CARTON (59779-574-08) > 24 TABLET in 1 BLISTER PACK |
Product NDC | 59779-574 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20080609 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
Substance Name | ACETAMINOPHEN; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 325; 200; 30 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |