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Excedrin
Excedrin - 0067-2035-24 - (Acetaminophen, Asprin, Caffeine)
Drug Information of Excedrin
| Product NDC: | 0067-2035 |
| Proprietary Name: | Excedrin |
| Non Proprietary Name: | Acetaminophen, Asprin, Caffeine |
| Active Ingredient(s): | 250; 250; 65 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Asprin, Caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Excedrin
| Product NDC: | 0067-2035 |
| Labeler Name: | Novartis Consumer Health, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020802 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110913 |
Package Information of Excedrin
| Package NDC: | 0067-2035-24 |
| Package Description: | 1 BOTTLE in 1 CARTON (0067-2035-24) > 24 TABLET, COATED in 1 BOTTLE |
NDC Information of Excedrin
| NDC Code | 0067-2035-24 |
| Proprietary Name | Excedrin |
| Package Description | 1 BOTTLE in 1 CARTON (0067-2035-24) > 24 TABLET, COATED in 1 BOTTLE |
| Product NDC | 0067-2035 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Asprin, Caffeine |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110913 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Consumer Health, Inc |
| Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
| Strength Number | 250; 250; 65 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
