"0093-3009-93" National Drug Code (NDC)

Lansoprazole 100 BLISTER PACK in 1 CARTON (0093-3009-93) > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK (0093-3009-19)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-3009-93
Package Description100 BLISTER PACK in 1 CARTON (0093-3009-93) > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK (0093-3009-19)
Product NDC0093-3009
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLansoprazole
Non-Proprietary NameLansoprazole
Dosage FormTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
UsageORAL
Start Marketing Date20180308
Marketing Category NameANDA
Application NumberANDA208784
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameLANSOPRAZOLE
Strength30
Strength Unitmg/1
Pharmacy ClassesInhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

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