Product NDC: | 59779-180 |
Proprietary Name: | ibuprofen cold relief |
Non Proprietary Name: | Ibuprofen, Pseudoephedrine HCl |
Active Ingredient(s): | 100; 15 mg/5mL; mg/5mL & nbsp; Ibuprofen, Pseudoephedrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-180 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA076478 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040212 |
Package NDC: | 59779-180-26 |
Package Description: | 1 BOTTLE in 1 CARTON (59779-180-26) > 120 mL in 1 BOTTLE |
NDC Code | 59779-180-26 |
Proprietary Name | ibuprofen cold relief |
Package Description | 1 BOTTLE in 1 CARTON (59779-180-26) > 120 mL in 1 BOTTLE |
Product NDC | 59779-180 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ibuprofen, Pseudoephedrine HCl |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20040212 |
Marketing Category Name | ANDA |
Labeler Name | CVS Pharmacy |
Substance Name | IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 100; 15 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |