Product NDC: | 41167-3102 |
Proprietary Name: | Premsyn pms Premenstrual Syndrome Relief |
Non Proprietary Name: | Acetaminophen and Pamabrom and Pyrilamine maleate |
Active Ingredient(s): | 500; 25; 15 mg/1; mg/1; mg/1 & nbsp; Acetaminophen and Pamabrom and Pyrilamine maleate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41167-3102 |
Labeler Name: | Chattem, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part357 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100501 |
Package NDC: | 41167-3102-3 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (41167-3102-3) > 40 TABLET in 1 BOTTLE, PLASTIC |
NDC Code | 41167-3102-3 |
Proprietary Name | Premsyn pms Premenstrual Syndrome Relief |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (41167-3102-3) > 40 TABLET in 1 BOTTLE, PLASTIC |
Product NDC | 41167-3102 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen and Pamabrom and Pyrilamine maleate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100501 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Chattem, Inc. |
Substance Name | ACETAMINOPHEN; PAMABROM; PYRILAMINE MALEATE |
Strength Number | 500; 25; 15 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |