Product NDC: | 55910-369 |
Proprietary Name: | Menstrual Pain Relief |
Non Proprietary Name: | Acetaminophen, Pamabrom and Pyrilamine maleate |
Active Ingredient(s): | 500; 25; 15 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Pamabrom and Pyrilamine maleate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55910-369 |
Labeler Name: | DOLGENCORP, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20000620 |
Package NDC: | 55910-369-27 |
Package Description: | 1 BOTTLE, GLASS in 1 CARTON (55910-369-27) > 32 TABLET, FILM COATED in 1 BOTTLE, GLASS |
NDC Code | 55910-369-27 |
Proprietary Name | Menstrual Pain Relief |
Package Description | 1 BOTTLE, GLASS in 1 CARTON (55910-369-27) > 32 TABLET, FILM COATED in 1 BOTTLE, GLASS |
Product NDC | 55910-369 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Pamabrom and Pyrilamine maleate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20000620 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | DOLGENCORP, LLC |
Substance Name | ACETAMINOPHEN; PAMABROM; PYRILAMINE MALEATE |
Strength Number | 500; 25; 15 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |