"69539-092-30" National Drug Code (NDC)

Erlotinib Hydrochloride 1 BOTTLE in 1 CARTON (69539-092-30) > 30 TABLET, FILM COATED in 1 BOTTLE
(MSN LABORATORIES PRIVATE LIMITED)

NDC Code69539-092-30
Package Description1 BOTTLE in 1 CARTON (69539-092-30) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC69539-092
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib Hydrochloride
Non-Proprietary NameErlotinib Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210511
Marketing Category NameANDA
Application NumberANDA214366
ManufacturerMSN LABORATORIES PRIVATE LIMITED
Substance NameERLOTINIB HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

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