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Pain Relief PM
Pain Relief PM - 63548-2341-1 - (Acetaminophen and Diphenhydramine Hydrochloride)
Drug Information of Pain Relief PM
| Product NDC: | 63548-2341 |
| Proprietary Name: | Pain Relief 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, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pain Relief PM
| Product NDC: | 63548-2341 |
| Labeler Name: | Avema Pharma Solutions |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100102 |
Package Information of Pain Relief PM
| Package NDC: | 63548-2341-1 |
| Package Description: | 24 TABLET, COATED in 1 BOTTLE, PLASTIC (63548-2341-1) |
NDC Information of Pain Relief PM
| NDC Code | 63548-2341-1 |
| Proprietary Name | Pain Relief PM |
| Package Description | 24 TABLET, COATED in 1 BOTTLE, PLASTIC (63548-2341-1) |
| Product NDC | 63548-2341 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and Diphenhydramine Hydrochloride |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100102 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Avema Pharma Solutions |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
