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mapap arthritis pain - 0904-5769-60 - (Acetaminophen)

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Drug Information of mapap arthritis pain

Product NDC: 0904-5769
Proprietary Name: mapap arthritis pain
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 mapap arthritis pain

Product NDC: 0904-5769
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075077
Marketing Category: ANDA
Start Marketing Date: 20060216

Package Information of mapap arthritis pain

Package NDC: 0904-5769-60
Package Description: 1 BOTTLE in 1 CARTON (0904-5769-60) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

NDC Information of mapap arthritis pain

NDC Code 0904-5769-60
Proprietary Name mapap arthritis pain
Package Description 1 BOTTLE in 1 CARTON (0904-5769-60) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC 0904-5769
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060216
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of mapap arthritis pain


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