Product NDC: | 11822-0373 |
Proprietary Name: | PM pain reliever |
Non Proprietary Name: | Acetaminophen and Diphenhydramine Citrate |
Active Ingredient(s): | 500; 38 mg/1; mg/1 & nbsp; Acetaminophen and Diphenhydramine Citrate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11822-0373 |
Labeler Name: | Rite Aid |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part338 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20040607 |
Package NDC: | 11822-0373-2 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (11822-0373-2) > 100 TABLET in 1 BOTTLE, PLASTIC |
NDC Code | 11822-0373-2 |
Proprietary Name | PM pain reliever |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (11822-0373-2) > 100 TABLET in 1 BOTTLE, PLASTIC |
Product NDC | 11822-0373 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen and Diphenhydramine Citrate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20040607 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Rite Aid |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE CITRATE |
Strength Number | 500; 38 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |