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Acetaminophen and Diphenhydramine HCl
Acetaminophen and Diphenhydramine HCl - 0536-3479-06 - (Acetaminophen and Diphenhydramine HCl)
Drug Information of Acetaminophen and Diphenhydramine HCl
| Product NDC: | 0536-3479 |
| Proprietary Name: | Acetaminophen and Diphenhydramine HCl |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acetaminophen and Diphenhydramine HCl
| Product NDC: | 0536-3479 |
| Labeler Name: | Rugby Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101006 |
Package Information of Acetaminophen and Diphenhydramine HCl
| Package NDC: | 0536-3479-06 |
| Package Description: | 50 TABLET in 1 BOTTLE (0536-3479-06) |
NDC Information of Acetaminophen and Diphenhydramine HCl
| NDC Code | 0536-3479-06 |
| Proprietary Name | Acetaminophen and Diphenhydramine HCl |
| Package Description | 50 TABLET in 1 BOTTLE (0536-3479-06) |
| Product NDC | 0536-3479 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and Diphenhydramine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101006 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rugby Laboratories Inc. |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
