"63304-096-11" National Drug Code (NDC)

Erlotinib 3 BLISTER PACK in 1 CARTON (63304-096-11) > 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-096-31)
(Sun Pharmaceutical Industries, Inc.)

NDC Code63304-096-11
Package Description3 BLISTER PACK in 1 CARTON (63304-096-11) > 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-096-31)
Product NDC63304-096
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
Strength100
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

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