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Acetaminophen - 21695-008-30 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 21695-008
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: 21695-008
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20070101

Package Information of Acetaminophen

Package NDC: 21695-008-30
Package Description: 30 TABLET in 1 BOTTLE (21695-008-30)

NDC Information of Acetaminophen

NDC Code 21695-008-30
Proprietary Name Acetaminophen
Package Description 30 TABLET in 1 BOTTLE (21695-008-30)
Product NDC 21695-008
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Rebel Distributors Corp
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


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