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"0069-3070-75" National Drug Code (NDC)

Zithromax 3 BLISTER PACK in 1 CARTON (0069-3070-75) / 3 TABLET, FILM COATED in 1 BLISTER PACK
(Pfizer Laboratories Div Pfizer Inc)

NDC Code0069-3070-75
Package Description3 BLISTER PACK in 1 CARTON (0069-3070-75) / 3 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0069-3070
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZithromax
Non-Proprietary NameAzithromycin Dihydrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20020524
Marketing Category NameNDA
Application NumberNDA050784
ManufacturerPfizer Laboratories Div Pfizer 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/0069-3070-75





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