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"21695-369-18" National Drug Code (NDC)
Zidovudine 18 TABLET, FILM COATED in 1 BOTTLE (21695-369-18)
(Rebel Distributors Corp)
NDC Code
21695-369-18
Package Description
18 TABLET, FILM COATED in 1 BOTTLE (21695-369-18)
Product NDC
21695-369
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Zidovudine
Non-Proprietary Name
Zidovudine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20090701
Marketing Category Name
ANDA
Application Number
ANDA077267
Manufacturer
Rebel Distributors Corp
Substance Name
ZIDOVUDINE
Strength
300
Strength Unit
mg/1
Pharmacy Classes
Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/21695-369-18