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"51991-890-33" National Drug Code (NDC)

Erlotinib 30 TABLET, FILM COATED in 1 BOTTLE (51991-890-33)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-890-33
Package Description30 TABLET, FILM COATED in 1 BOTTLE (51991-890-33)
Product NDC51991-890
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib
Non-Proprietary NameErlotinib Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20191105
End Marketing Date20250731
Marketing Category NameANDA
Application NumberANDA208488
ManufacturerBreckenridge Pharmaceutical, 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/51991-890-33





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