| 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 |