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"63304-135-30" National Drug Code (NDC)

Erlotinib 30 TABLET, FILM COATED in 1 BOTTLE (63304-135-30)
(Sun Pharmaceutical Industries, Inc.)

NDC Code63304-135-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (63304-135-30)
Product NDC63304-135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib
Non-Proprietary NameErlotinib
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20191105
Marketing Category NameANDA
Application NumberANDA210300
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameERLOTINIB
Strength150
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63304-135-30





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