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Extra Strength Pain Relief - 50844-519-15 - (Acetaminophen)

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Drug Information of Extra Strength Pain Relief

Product NDC: 50844-519
Proprietary Name: Extra Strength Pain Relief
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 Relief

Product NDC: 50844-519
Labeler Name: L.N.K. International, 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 Relief

Package NDC: 50844-519-15
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (50844-519-15) > 50 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC

NDC Information of Extra Strength Pain Relief

NDC Code 50844-519-15
Proprietary Name Extra Strength Pain Relief
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (50844-519-15) > 50 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC
Product NDC 50844-519
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 L.N.K. International, Inc.
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Extra Strength Pain Relief


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