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"49348-921-09" National Drug Code (NDC)

Sunmark Arthritis Pain Reliever 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-921-09)
(Sunmark)

NDC Code49348-921-09
Package Description50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-921-09)
Product NDC49348-921
Product Type NameHUMAN OTC DRUG
Proprietary NameSunmark Arthritis Pain Reliever
Non-Proprietary NameAcetaminophen
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20020430
Marketing Category NameANDA
Application NumberANDA076200
ManufacturerSunmark
Substance NameACETAMINOPHEN
Strength650
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49348-921-09





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