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Acetaminophen - 0536-3233-07 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 0536-3233
Proprietary Name: Acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 80    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen

Product NDC: 0536-3233
Labeler Name: Rugby Laboratories Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20020812

Package Information of Acetaminophen

Package NDC: 0536-3233-07
Package Description: 30 TABLET in 1 BOTTLE (0536-3233-07)

NDC Information of Acetaminophen

NDC Code 0536-3233-07
Proprietary Name Acetaminophen
Package Description 30 TABLET in 1 BOTTLE (0536-3233-07)
Product NDC 0536-3233
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020812
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rugby Laboratories Inc.
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen

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