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"52125-068-02" National Drug Code (NDC)

Zithromax 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-068-02)
(REMEDYREPACK INC.)

NDC Code52125-068-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (52125-068-02)
Product NDC52125-068
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZithromax
Non-Proprietary NameAzithromycin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130312
Marketing Category NameNDA
Application NumberNDA050711
ManufacturerREMEDYREPACK INC.
Substance NameAZITHROMYCIN, UNSPECIFIED FORM
Strength250
Strength Unitmg/1
Pharmacy ClassesMacrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-068-02





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