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"61786-305-02" National Drug Code (NDC)
Zidovudine 30 TABLET, FILM COATED in 1 BLISTER PACK (61786-305-02)
(REMEDYREPACK INC.)
NDC Code
61786-305-02
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (61786-305-02)
Product NDC
61786-305
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Zidovudine
Non-Proprietary Name
Zidovudine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20150526
Marketing Category Name
ANDA
Application Number
ANDA202058
Manufacturer
REMEDYREPACK INC.
Substance Name
ZIDOVUDINE
Strength
300
Strength Unit
mg/1
Pharmacy Classes
Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61786-305-02