Product NDC: | 55319-556 |
Proprietary Name: | Extra Strength Acetaminophen PM |
Non Proprietary Name: | Acetaminophen and Diphenhydramine HCl |
Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; Acetaminophen and Diphenhydramine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55319-556 |
Labeler Name: | Family Dollar |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20071217 |
Package NDC: | 55319-556-09 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (55319-556-09) > 20 CAPSULE in 1 BOTTLE, PLASTIC |
NDC Code | 55319-556-09 |
Proprietary Name | Extra Strength Acetaminophen PM |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (55319-556-09) > 20 CAPSULE in 1 BOTTLE, PLASTIC |
Product NDC | 55319-556 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen and Diphenhydramine HCl |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20071217 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Family Dollar |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 500; 25 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |