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"0093-7222-10" National Drug Code (NDC)

Fosinopril Sodium 1000 TABLET in 1 BOTTLE (0093-7222-10)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7222-10
Package Description1000 TABLET in 1 BOTTLE (0093-7222-10)
Product NDC0093-7222
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFosinopril Sodium
Non-Proprietary NameFosinopril Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20031201
End Marketing Date20191231
Marketing Category NameANDA
Application NumberANDA076139
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameFOSINOPRIL SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-7222-10





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