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Tylenol PM
Tylenol PM - 50580-482-32 - (Acetaminophen and Diphenhydramine Hydrochloride)
Drug Information of Tylenol PM
| Product NDC: | 50580-482 |
| Proprietary Name: | Tylenol PM |
| Non Proprietary Name: | Acetaminophen and Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; Acetaminophen and Diphenhydramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tylenol PM
| Product NDC: | 50580-482 |
| Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part338 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19910424 |
Package Information of Tylenol PM
| Package NDC: | 50580-482-32 |
| Package Description: | 12 VIAL, PLASTIC in 1 CARTON (50580-482-32) > 10 TABLET, FILM COATED in 1 VIAL, PLASTIC |
NDC Information of Tylenol PM
| NDC Code | 50580-482-32 |
| Proprietary Name | Tylenol PM |
| Package Description | 12 VIAL, PLASTIC in 1 CARTON (50580-482-32) > 10 TABLET, FILM COATED in 1 VIAL, PLASTIC |
| Product NDC | 50580-482 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and Diphenhydramine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19910424 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
