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Sunmark 8 hour pain relief - 49348-705-09 - (Acetaminophen)

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Drug Information of Sunmark 8 hour pain relief

Product NDC: 49348-705
Proprietary Name: Sunmark 8 hour 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 Sunmark 8 hour pain relief

Product NDC: 49348-705
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075077
Marketing Category: ANDA
Start Marketing Date: 20050830

Package Information of Sunmark 8 hour pain relief

Package NDC: 49348-705-09
Package Description: 1 BOTTLE in 1 CARTON (49348-705-09) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

NDC Information of Sunmark 8 hour pain relief

NDC Code 49348-705-09
Proprietary Name Sunmark 8 hour pain relief
Package Description 1 BOTTLE in 1 CARTON (49348-705-09) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC 49348-705
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20050830
Marketing Category Name ANDA
Labeler Name McKesson
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Sunmark 8 hour pain relief


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