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Acetaminophen - 17714-012-10 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 17714-012
Proprietary Name: Acetaminophen
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 Acetaminophen

Product NDC: 17714-012
Labeler Name: Advance Pharmaceutical Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19890205

Package Information of Acetaminophen

Package NDC: 17714-012-10
Package Description: 1000 TABLET in 1 BOTTLE (17714-012-10)

NDC Information of Acetaminophen

NDC Code 17714-012-10
Proprietary Name Acetaminophen
Package Description 1000 TABLET in 1 BOTTLE (17714-012-10)
Product NDC 17714-012
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19890205
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Advance Pharmaceutical Inc.
Substance Name ACETAMINOPHEN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


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