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Extra Strength Pain Reliever - 55315-519-15 - (Acetaminophen)

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Drug Information of Extra Strength Pain Reliever

Product NDC: 55315-519
Proprietary Name: Extra Strength Pain Reliever
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Extra Strength Pain Reliever

Product NDC: 55315-519
Labeler Name: FRED'S, INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20040510

Package Information of Extra Strength Pain Reliever

Package NDC: 55315-519-15
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (55315-519-15) > 50 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC

NDC Information of Extra Strength Pain Reliever

NDC Code 55315-519-15
Proprietary Name Extra Strength Pain Reliever
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (55315-519-15) > 50 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC
Product NDC 55315-519
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20040510
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name FRED'S, INC.
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Extra Strength Pain Reliever


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