Product NDC: | 56062-374 |
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 |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 56062-374 |
Labeler Name: | Publix Super Markets Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075794 |
Marketing Category: | ANDA |
Start Marketing Date: | 20021226 |
Package NDC: | 56062-374-71 |
Package Description: | 1 BOTTLE in 1 CARTON (56062-374-71) > 50 TABLET in 1 BOTTLE |
NDC Code | 56062-374-71 |
Proprietary Name | migraine relief |
Package Description | 1 BOTTLE in 1 CARTON (56062-374-71) > 50 TABLET in 1 BOTTLE |
Product NDC | 56062-374 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Aspirin, Caffeine |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20021226 |
Marketing Category Name | ANDA |
Labeler Name | Publix Super Markets Inc |
Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
Strength Number | 250; 250; 65 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |