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"51224-122-09" National Drug Code (NDC)

Azithromycin Dihydrate 3 CARTON in 1 BOX (51224-122-09) > 1 BLISTER PACK in 1 CARTON (51224-122-03) > 3 TABLET, FILM COATED in 1 BLISTER PACK
(TAGI Pharma, Inc.)

NDC Code51224-122-09
Package Description3 CARTON in 1 BOX (51224-122-09) > 1 BLISTER PACK in 1 CARTON (51224-122-03) > 3 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC51224-122
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAzithromycin Dihydrate
Non-Proprietary NameAzithromycin Dihydrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190701
Marketing Category NameANDA
Application NumberANDA208249
ManufacturerTAGI Pharma, Inc.
Substance NameAZITHROMYCIN DIHYDRATE
Strength500
Strength Unitmg/1
Pharmacy ClassesMacrolide Antimicrobial [EPC], Macrolides [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51224-122-09





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