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Extra Strength Pain Relief - 11822-0104-1 - (Acetaminophen)

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Drug Information of Extra Strength Pain Relief

Product NDC: 11822-0104
Proprietary Name: Extra Strength Pain Relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 325    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Extra Strength Pain Relief

Product NDC: 11822-0104
Labeler Name: Rite Aid
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19900713

Package Information of Extra Strength Pain Relief

Package NDC: 11822-0104-1
Package Description: 1 BOTTLE in 1 CARTON (11822-0104-1) > 100 TABLET in 1 BOTTLE

NDC Information of Extra Strength Pain Relief

NDC Code 11822-0104-1
Proprietary Name Extra Strength Pain Relief
Package Description 1 BOTTLE in 1 CARTON (11822-0104-1) > 100 TABLET in 1 BOTTLE
Product NDC 11822-0104
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900713
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Rite Aid
Substance Name ACETAMINOPHEN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Extra Strength Pain Relief


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