"0093-2203-05" National Drug Code (NDC)

Metoclopramide 500 TABLET in 1 BOTTLE (0093-2203-05)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-2203-05
Package Description500 TABLET in 1 BOTTLE (0093-2203-05)
Product NDC0093-2203
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoclopramide
Non-Proprietary NameMetoclopramide
Dosage FormTABLET
UsageORAL
Start Marketing Date19900930
Marketing Category NameANDA
Application NumberANDA070184
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameMETOCLOPRAMIDE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesDopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]

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