Product NDC: | 0363-0213 |
Proprietary Name: | Pain Reliever PM |
Non Proprietary Name: | Acetaminophen, Diphenhydramine HCl |
Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0363-0213 |
Labeler Name: | Walgreens |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130531 |
Package NDC: | 0363-0213-10 |
Package Description: | 1 BOTTLE, PLASTIC in 1 BOX (0363-0213-10) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
NDC Code | 0363-0213-10 |
Proprietary Name | Pain Reliever PM |
Package Description | 1 BOTTLE, PLASTIC in 1 BOX (0363-0213-10) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
Product NDC | 0363-0213 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Diphenhydramine HCl |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20130531 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Walgreens |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 500; 25 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |