Product NDC: | 59779-891 |
Proprietary Name: | cold and sinus relief |
Non Proprietary Name: | Ibuprofen, Pseudoephedrine Hydrochloride |
Active Ingredient(s): | 200; 30 mg/1; mg/1 & nbsp; Ibuprofen, Pseudoephedrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, SUGAR COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-891 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA074567 |
Marketing Category: | ANDA |
Start Marketing Date: | 20011009 |
Package NDC: | 59779-891-60 |
Package Description: | 2 BLISTER PACK in 1 CARTON (59779-891-60) > 10 TABLET, SUGAR COATED in 1 BLISTER PACK |
NDC Code | 59779-891-60 |
Proprietary Name | cold and sinus relief |
Package Description | 2 BLISTER PACK in 1 CARTON (59779-891-60) > 10 TABLET, SUGAR COATED in 1 BLISTER PACK |
Product NDC | 59779-891 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ibuprofen, Pseudoephedrine Hydrochloride |
Dosage Form Name | TABLET, SUGAR COATED |
Route Name | ORAL |
Start Marketing Date | 20011009 |
Marketing Category Name | ANDA |
Labeler Name | CVS Pharmacy |
Substance Name | IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 200; 30 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |