Product NDC: | 52904-468 |
Proprietary Name: | Pain Relief Maximum Strength |
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, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52904-468 |
Labeler Name: | Select Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121015 |
Package NDC: | 52904-468-02 |
Package Description: | 2 TABLET, COATED in 1 PACKET (52904-468-02) |
NDC Code | 52904-468-02 |
Proprietary Name | Pain Relief Maximum Strength |
Package Description | 2 TABLET, COATED in 1 PACKET (52904-468-02) |
Product NDC | 52904-468 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen,Aspirin,Caffeine |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20121015 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Select Corporation |
Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
Strength Number | 250; 250; 65 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |