"61919-555-06" National Drug Code (NDC)

Zithromax 1 TABLET, FILM COATED in 1 BOTTLE (61919-555-06)
(DIRECT RX)

NDC Code61919-555-06
Package Description1 TABLET, FILM COATED in 1 BOTTLE (61919-555-06)
Product NDC61919-555
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZithromax
Non-Proprietary NameAzithromycin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160302
Marketing Category NameANDA
Application NumberANDA065404
ManufacturerDIRECT RX
Substance NameAZITHROMYCIN ANHYDROUS
Strength250
Strength Unitmg/1
Pharmacy ClassesMacrolide Antimicrobial [EPC], Macrolides [CS]

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