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Acetaminophen - 15127-175-08 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 15127-175
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: 15127-175
Labeler Name: Stephen L. LaFrance Pharmacy, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19930402

Package Information of Acetaminophen

Package NDC: 15127-175-08
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (15127-175-08) > 24 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Acetaminophen

NDC Code 15127-175-08
Proprietary Name Acetaminophen
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (15127-175-08) > 24 TABLET in 1 BOTTLE, PLASTIC
Product NDC 15127-175
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930402
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Stephen L. LaFrance Pharmacy, Inc.
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


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