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Headache Relief - 70253-159-12 - (Acetaminophen, Aspirin and caffeine)

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Drug Information of Headache Relief

Product NDC: 70253-159
Proprietary Name: 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 Headache Relief

Product NDC: 70253-159
Labeler Name: NASH-FINCH COMPANY
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19921117

Package Information of Headache Relief

Package NDC: 70253-159-12
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (70253-159-12) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Headache Relief

NDC Code 70253-159-12
Proprietary Name Headache Relief
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (70253-159-12) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 70253-159
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 NASH-FINCH COMPANY
Substance Name ACETAMINOPHEN; ASPIRIN; CAFFEINE
Strength Number 250; 250; 65
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Headache Relief


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