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PM Acetaminophen
PM Acetaminophen - 51824-016-05 - (Diphenhydramine Hydrochloride, Acetaminophen)
Drug Information of PM Acetaminophen
| Product NDC: | 51824-016 |
| Proprietary Name: | PM Acetaminophen |
| Non Proprietary Name: | Diphenhydramine Hydrochloride, Acetaminophen |
| Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; Diphenhydramine Hydrochloride, Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PM Acetaminophen
| Product NDC: | 51824-016 |
| Labeler Name: | New World Imports, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111117 |
Package Information of PM Acetaminophen
| Package NDC: | 51824-016-05 |
| Package Description: | 50 TABLET in 1 BOTTLE (51824-016-05) |
NDC Information of PM Acetaminophen
| NDC Code | 51824-016-05 |
| Proprietary Name | PM Acetaminophen |
| Package Description | 50 TABLET in 1 BOTTLE (51824-016-05) |
| Product NDC | 51824-016 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride, Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111117 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | New World Imports, Inc |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
