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"59651-530-03" National Drug Code (NDC)
Erlotinib 30 TABLET, FILM COATED in 1 BOTTLE (59651-530-03)
(Aurobindo Pharma Limited)
NDC Code
59651-530-03
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (59651-530-03)
Product NDC
59651-530
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Erlotinib
Non-Proprietary Name
Erlotinib
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220622
Marketing Category Name
ANDA
Application Number
ANDA216342
Manufacturer
Aurobindo Pharma Limited
Substance Name
ERLOTINIB HYDROCHLORIDE
Strength
25
Strength Unit
mg/1
Pharmacy Classes
Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59651-530-03