Product NDC: | 10158-999 |
Proprietary Name: | Goodys |
Non Proprietary Name: | acetaminophen and aspirin |
Active Ingredient(s): | 325; 500 mg/1; mg/1 & nbsp; acetaminophen and aspirin |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10158-999 |
Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110817 |
Package NDC: | 10158-999-26 |
Package Description: | 24 POWDER in 1 CARTON (10158-999-26) |
NDC Code | 10158-999-26 |
Proprietary Name | Goodys |
Package Description | 24 POWDER in 1 CARTON (10158-999-26) |
Product NDC | 10158-999 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | acetaminophen and aspirin |
Dosage Form Name | POWDER |
Route Name | ORAL |
Start Marketing Date | 20110817 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
Substance Name | ACETAMINOPHEN; ASPIRIN |
Strength Number | 325; 500 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |