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Pain Relief PM
Pain Relief PM - 59779-373-08 - (Acetaminophen and Diphenhydramine Citrate)
Drug Information of Pain Relief PM
| Product NDC: | 59779-373 |
| Proprietary Name: | Pain Relief PM |
| 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) |
Labeler Information of Pain Relief PM
| Product NDC: | 59779-373 |
| Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part338 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040607 |
Package Information of Pain Relief PM
| Package NDC: | 59779-373-08 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (59779-373-08) > 24 TABLET in 1 BOTTLE, PLASTIC |
NDC Information of Pain Relief PM
| NDC Code | 59779-373-08 |
| Proprietary Name | Pain Relief PM |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (59779-373-08) > 24 TABLET in 1 BOTTLE, PLASTIC |
| Product NDC | 59779-373 |
| 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 | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE CITRATE |
| Strength Number | 500; 38 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
