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"67184-0531-3" National Drug Code (NDC)
Gefitinib 3 BLISTER PACK in 1 CARTON (67184-0531-3) / 10 TABLET, COATED in 1 BLISTER PACK
(Qilu Pharmaceutical Co., Ltd.)
NDC Code
67184-0531-3
Package Description
3 BLISTER PACK in 1 CARTON (67184-0531-3) / 10 TABLET, COATED in 1 BLISTER PACK
Product NDC
67184-0531
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gefitinib
Non-Proprietary Name
Gefitinib
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20230213
Marketing Category Name
ANDA
Application Number
ANDA211591
Manufacturer
Qilu Pharmaceutical Co., Ltd.
Substance Name
GEFITINIB
Strength
250
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/67184-0531-3