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"49348-704-10" National Drug Code (NDC)

Sunmark Arthritis Pain Relief 1 BOTTLE in 1 CARTON (49348-704-10) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
(McKesson)

NDC Code49348-704-10
Package Description1 BOTTLE in 1 CARTON (49348-704-10) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC49348-704
Product Type NameHUMAN OTC DRUG
Proprietary NameSunmark Arthritis Pain Relief
Non-Proprietary NameAcetaminophen
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20080213
Marketing Category NameANDA
Application NumberANDA075077
ManufacturerMcKesson
Substance NameACETAMINOPHEN
Strength650
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49348-704-10





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