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Excedrin
Excedrin - 0067-2053-84 - (Acetaminophen, Diphenhydramine Citrate)
Drug Information of Excedrin
| Product NDC: | 0067-2053 |
| Proprietary Name: | Excedrin |
| Non Proprietary Name: | Acetaminophen, Diphenhydramine Citrate |
| Active Ingredient(s): | 500; 38 mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine Citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Excedrin
| Product NDC: | 0067-2053 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100301 |
Package Information of Excedrin
| Package NDC: | 0067-2053-84 |
| Package Description: | 125 TABLET in 1 BOTTLE, PLASTIC (0067-2053-84) |
NDC Information of Excedrin
| NDC Code | 0067-2053-84 |
| Proprietary Name | Excedrin |
| Package Description | 125 TABLET in 1 BOTTLE, PLASTIC (0067-2053-84) |
| Product NDC | 0067-2053 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Diphenhydramine Citrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE CITRATE |
| Strength Number | 500; 38 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
