Product NDC: | 55910-390 |
Proprietary Name: | Maximum Strength Menstrual Relief |
Non Proprietary Name: | Acetaminophen, Caffeine and Pyrilamine maleate |
Active Ingredient(s): | 500; 60; 15 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Caffeine and Pyrilamine maleate |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55910-390 |
Labeler Name: | DOLGENCORP, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20020429 |
Package NDC: | 55910-390-10 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (55910-390-10) > 40 CAPSULE in 1 BOTTLE, PLASTIC |
NDC Code | 55910-390-10 |
Proprietary Name | Maximum Strength Menstrual Relief |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (55910-390-10) > 40 CAPSULE in 1 BOTTLE, PLASTIC |
Product NDC | 55910-390 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Caffeine and Pyrilamine maleate |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20020429 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | DOLGENCORP, LLC |
Substance Name | ACETAMINOPHEN; CAFFEINE; PYRILAMINE MALEATE |
Strength Number | 500; 60; 15 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |