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"72485-217-30" National Drug Code (NDC)
Erlotinib 1 BOTTLE in 1 BOX (72485-217-30) > 30 TABLET, FILM COATED in 1 BOTTLE
(Armas Pharmaceuticals Inc.)
NDC Code
72485-217-30
Package Description
1 BOTTLE in 1 BOX (72485-217-30) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC
72485-217
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Erlotinib
Non-Proprietary Name
Erlotinib Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20191106
Marketing Category Name
ANDA
Application Number
ANDA211960
Manufacturer
Armas Pharmaceuticals Inc.
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/72485-217-30