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ACETAMINOPHEN - 65437-040-31 - (ACETAMINOPHEN)

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Drug Information of ACETAMINOPHEN

Product NDC: 65437-040
Proprietary Name: ACETAMINOPHEN
Non Proprietary Name: ACETAMINOPHEN
Active Ingredient(s): 500    mg/1 & nbsp;   ACETAMINOPHEN
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ACETAMINOPHEN

Product NDC: 65437-040
Labeler Name: HIMPRIT PHARMACHEM PVT LTD
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100701

Package Information of ACETAMINOPHEN

Package NDC: 65437-040-31
Package Description: 1 BAG in 1 DRUM (65437-040-31) > 31000 TABLET, FILM COATED in 1 BAG

NDC Information of ACETAMINOPHEN

NDC Code 65437-040-31
Proprietary Name ACETAMINOPHEN
Package Description 1 BAG in 1 DRUM (65437-040-31) > 31000 TABLET, FILM COATED in 1 BAG
Product NDC 65437-040
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100701
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name HIMPRIT PHARMACHEM PVT LTD
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ACETAMINOPHEN


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