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"61919-555-06" National Drug Code (NDC)
Zithromax 1 TABLET, FILM COATED in 1 BOTTLE (61919-555-06)
(DIRECT RX)
NDC Code
61919-555-06
Package Description
1 TABLET, FILM COATED in 1 BOTTLE (61919-555-06)
Product NDC
61919-555
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Zithromax
Non-Proprietary Name
Azithromycin
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20160302
Marketing Category Name
ANDA
Application Number
ANDA065404
Manufacturer
DIRECT RX
Substance Name
AZITHROMYCIN ANHYDROUS
Strength
250
Strength Unit
mg/1
Pharmacy Classes
Macrolide Antimicrobial [EPC], Macrolides [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-555-06