Product NDC: | 0498-2520 |
Proprietary Name: | Pain Stoppers Extra |
Non Proprietary Name: | Acetaminophen, Caffeine, Aspirin |
Active Ingredient(s): | 250; 250; 65 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Caffeine, Aspirin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0498-2520 |
Labeler Name: | North Safety Products LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120307 |
Package NDC: | 0498-2520-50 |
Package Description: | 250 CARTON in 1 CARTON (0498-2520-50) > 125 CARTON in 1 CARTON (0498-2520-25) > 50 PACKET in 1 CARTON (0498-2520-10) > 2 TABLET, COATED in 1 PACKET (0498-2520-01) |
NDC Code | 0498-2520-50 |
Proprietary Name | Pain Stoppers Extra |
Package Description | 250 CARTON in 1 CARTON (0498-2520-50) > 125 CARTON in 1 CARTON (0498-2520-25) > 50 PACKET in 1 CARTON (0498-2520-10) > 2 TABLET, COATED in 1 PACKET (0498-2520-01) |
Product NDC | 0498-2520 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Caffeine, Aspirin |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20120307 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | North Safety Products LLC |
Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
Strength Number | 250; 250; 65 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |