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arthritis pain relief - 41250-966-47 - (Acetaminophen)

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Drug Information of arthritis pain relief

Product NDC: 41250-966
Proprietary Name: arthritis pain relief
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 arthritis pain relief

Product NDC: 41250-966
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075077
Marketing Category: ANDA
Start Marketing Date: 20070905

Package Information of arthritis pain relief

Package NDC: 41250-966-47
Package Description: 150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (41250-966-47)

NDC Information of arthritis pain relief

NDC Code 41250-966-47
Proprietary Name arthritis pain relief
Package Description 150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (41250-966-47)
Product NDC 41250-966
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070905
Marketing Category Name ANDA
Labeler Name Meijer Distribution Inc
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of arthritis pain relief


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