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"70518-0249-0" National Drug Code (NDC)

Zithromax 6 TABLET, FILM COATED in 1 BLISTER PACK (70518-0249-0)
(REMEDYREPACK INC.)

NDC Code70518-0249-0
Package Description6 TABLET, FILM COATED in 1 BLISTER PACK (70518-0249-0)
Product NDC70518-0249
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZithromax
Non-Proprietary NameAzithromycin Dihydrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170222
Marketing Category NameNDA
Application NumberNDA050711
ManufacturerREMEDYREPACK INC.
Substance NameAZITHROMYCIN DIHYDRATE
Strength250
Strength Unitmg/1
Pharmacy ClassesMacrolide Antimicrobial [EPC], Macrolides [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0249-0





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