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Acetaminophen - 63868-091-01 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 63868-091
Proprietary Name: Acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 650    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen

Product NDC: 63868-091
Labeler Name: Chain Drug Marketing Association Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076200
Marketing Category: ANDA
Start Marketing Date: 20020430

Package Information of Acetaminophen

Package NDC: 63868-091-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63868-091-01)

NDC Information of Acetaminophen

NDC Code 63868-091-01
Proprietary Name Acetaminophen
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63868-091-01)
Product NDC 63868-091
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20020430
Marketing Category Name ANDA
Labeler Name Chain Drug Marketing Association Inc.
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


General Information