 
                        | Product NDC: | 0363-0374 | 
| Proprietary Name: | migraine relief | 
| Non Proprietary Name: | Acetaminophen, Aspirin, Caffeine | 
| Active Ingredient(s): | 250; 250; 65 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Aspirin, Caffeine | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, FILM COATED | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0363-0374 | 
| Labeler Name: | Walgreen Company | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | ANDA075794 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20020502 | 
| Package NDC: | 0363-0374-85 | 
| Package Description: | 250 TABLET, FILM COATED in 1 BOTTLE (0363-0374-85) | 
| NDC Code | 0363-0374-85 | 
| Proprietary Name | migraine relief | 
| Package Description | 250 TABLET, FILM COATED in 1 BOTTLE (0363-0374-85) | 
| Product NDC | 0363-0374 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Acetaminophen, Aspirin, Caffeine | 
| Dosage Form Name | TABLET, FILM COATED | 
| Route Name | ORAL | 
| Start Marketing Date | 20020502 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Walgreen Company | 
| Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE | 
| Strength Number | 250; 250; 65 | 
| Strength Unit | mg/1; mg/1; mg/1 | 
| Pharmaceutical Classes |