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Acetaminophen - 63739-440-01 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 63739-440
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: 63739-440
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED OTHER
Start Marketing Date: 20090428

Package Information of Acetaminophen

Package NDC: 63739-440-01
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-440-01) > 30 TABLET in 1 BLISTER PACK

NDC Information of Acetaminophen

NDC Code 63739-440-01
Proprietary Name Acetaminophen
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-440-01) > 30 TABLET in 1 BLISTER PACK
Product NDC 63739-440
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090428
Marketing Category Name UNAPPROVED OTHER
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name ACETAMINOPHEN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


General Information