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Excedrin Extra Strength
Excedrin Extra Strength - 66715-9710-8 - (Acetaminophen, Aspirin, and Caffeine)
Drug Information of Excedrin Extra Strength
| Product NDC: | 66715-9710 |
| Proprietary Name: | Excedrin Extra Strength |
| Non Proprietary Name: | Acetaminophen, Aspirin, and Caffeine |
| Active Ingredient(s): | 250; 250; 65 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Aspirin, and Caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Excedrin Extra Strength
| Product NDC: | 66715-9710 |
| Labeler Name: | Lil' Drug Store Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100510 |
Package Information of Excedrin Extra Strength
| Package NDC: | 66715-9710-8 |
| Package Description: | 6 POUCH in 1 CARTON (66715-9710-8) > 2 TABLET in 1 POUCH |
NDC Information of Excedrin Extra Strength
| NDC Code | 66715-9710-8 |
| Proprietary Name | Excedrin Extra Strength |
| Package Description | 6 POUCH in 1 CARTON (66715-9710-8) > 2 TABLET in 1 POUCH |
| Product NDC | 66715-9710 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Aspirin, and Caffeine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100510 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Lil' Drug Store Products, Inc. |
| Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
| Strength Number | 250; 250; 65 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
