Product NDC: | 0135-0462 |
Proprietary Name: | Goodys |
Non Proprietary Name: | acetaminophen, aspirin, and caffeine |
Active Ingredient(s): | 325; 500; 65 mg/1; mg/1; mg/1 & nbsp; acetaminophen, aspirin, and caffeine |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0135-0462 |
Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110923 |
Package NDC: | 0135-0462-03 |
Package Description: | 1 POWDER in 1 PACKAGE (0135-0462-03) |
NDC Code | 0135-0462-03 |
Proprietary Name | Goodys |
Package Description | 1 POWDER in 1 PACKAGE (0135-0462-03) |
Product NDC | 0135-0462 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | acetaminophen, aspirin, and caffeine |
Dosage Form Name | POWDER |
Route Name | ORAL |
Start Marketing Date | 20110923 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
Strength Number | 325; 500; 65 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |