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Wal-Nadol PM
Wal-Nadol PM - 0363-0235-57 - (Acetaminophen and Diphenhydramine HCl)
Drug Information of Wal-Nadol PM
| Product NDC: | 0363-0235 |
| Proprietary Name: | Wal-Nadol 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): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Wal-Nadol PM
| Product NDC: | 0363-0235 |
| Labeler Name: | WALGREEN CO. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19940515 |
Package Information of Wal-Nadol PM
| Package NDC: | 0363-0235-57 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0363-0235-57) > 125 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
NDC Information of Wal-Nadol PM
| NDC Code | 0363-0235-57 |
| Proprietary Name | Wal-Nadol PM |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0363-0235-57) > 125 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| Product NDC | 0363-0235 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and Diphenhydramine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19940515 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | WALGREEN CO. |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
