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Sunmark Arthritis Pain Reliever - 49348-921-10 - (Acetaminophen)

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Drug Information of Sunmark Arthritis Pain Reliever

Product NDC: 49348-921
Proprietary Name: Sunmark Arthritis Pain Reliever
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 Sunmark Arthritis Pain Reliever

Product NDC: 49348-921
Labeler Name: Sunmark
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076200
Marketing Category: ANDA
Start Marketing Date: 20020430

Package Information of Sunmark Arthritis Pain Reliever

Package NDC: 49348-921-10
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-921-10)

NDC Information of Sunmark Arthritis Pain Reliever

NDC Code 49348-921-10
Proprietary Name Sunmark Arthritis Pain Reliever
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-921-10)
Product NDC 49348-921
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 Sunmark
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Sunmark Arthritis Pain Reliever


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