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Extra Strength Headache Relief
Extra Strength Headache Relief - 37205-669-78 - (Acetaminophen, Aspirin and caffeine)
Drug Information of Extra Strength Headache Relief
| Product NDC: | 37205-669 |
| Proprietary Name: | Extra Strength Headache Relief |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Extra Strength Headache Relief
| Product NDC: | 37205-669 |
| Labeler Name: | CARDINAL HEALTH |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19921117 |
Package Information of Extra Strength Headache Relief
| Package NDC: | 37205-669-78 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (37205-669-78) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
NDC Information of Extra Strength Headache Relief
| NDC Code | 37205-669-78 |
| Proprietary Name | Extra Strength Headache Relief |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37205-669-78) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| Product NDC | 37205-669 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Aspirin and caffeine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19921117 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CARDINAL HEALTH |
| Substance Name | ACETAMINOPHEN; ASPIRIN; CAFFEINE |
| Strength Number | 250; 250; 65 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
