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Acetaminophen - 11822-0227-1 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 11822-0227
Proprietary Name: Acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen

Product NDC: 11822-0227
Labeler Name: Rite Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20051107

Package Information of Acetaminophen

Package NDC: 11822-0227-1
Package Description: 1 BOTTLE in 1 CARTON (11822-0227-1) > 50 TABLET, COATED in 1 BOTTLE

NDC Information of Acetaminophen

NDC Code 11822-0227-1
Proprietary Name Acetaminophen
Package Description 1 BOTTLE in 1 CARTON (11822-0227-1) > 50 TABLET, COATED in 1 BOTTLE
Product NDC 11822-0227
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20051107
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Rite Aid Corporation
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


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