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Topcare Arthritis Pain Relief - 36800-544-78 - (Acetaminophen)

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Drug Information of Topcare Arthritis Pain Relief

Product NDC: 36800-544
Proprietary Name: Topcare 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 Topcare Arthritis Pain Relief

Product NDC: 36800-544
Labeler Name: Topco Associates LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075077
Marketing Category: ANDA
Start Marketing Date: 20050804

Package Information of Topcare Arthritis Pain Relief

Package NDC: 36800-544-78
Package Description: 1 BOTTLE in 1 CARTON (36800-544-78) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

NDC Information of Topcare Arthritis Pain Relief

NDC Code 36800-544-78
Proprietary Name Topcare Arthritis Pain Relief
Package Description 1 BOTTLE in 1 CARTON (36800-544-78) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC 36800-544
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20050804
Marketing Category Name ANDA
Labeler Name Topco Associates LLC
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Topcare Arthritis Pain Relief


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