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"62332-565-30" National Drug Code (NDC)

Erlotinib Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (62332-565-30)
(Alembic Pharmaceuticals Inc.)

NDC Code62332-565-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (62332-565-30)
Product NDC62332-565
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib Hydrochloride
Non-Proprietary NameErlotinib Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210709
Marketing Category NameANDA
Application NumberANDA214719
ManufacturerAlembic Pharmaceuticals Inc.
Substance NameERLOTINIB HYDROCHLORIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/62332-565-30





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