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acetaminophen - 55312-484-71 - (Acetaminophen)

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Drug Information of acetaminophen

Product NDC: 55312-484
Proprietary Name: acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of acetaminophen

Product NDC: 55312-484
Labeler Name: Western Family Foods Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20080314

Package Information of acetaminophen

Package NDC: 55312-484-71
Package Description: 1 BOTTLE in 1 CARTON (55312-484-71) > 50 TABLET in 1 BOTTLE

NDC Information of acetaminophen

NDC Code 55312-484-71
Proprietary Name acetaminophen
Package Description 1 BOTTLE in 1 CARTON (55312-484-71) > 50 TABLET in 1 BOTTLE
Product NDC 55312-484
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080314
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Western Family Foods Inc
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of acetaminophen


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