"16571-772-10" National Drug Code (NDC)

Fosinopril Sodium 1000 TABLET in 1 BOTTLE (16571-772-10)
(Rising Pharma Holdings, Inc.)

NDC Code16571-772-10
Package Description1000 TABLET in 1 BOTTLE (16571-772-10)
Product NDC16571-772
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFosinopril Sodium
Non-Proprietary NameFosinopril Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20110330
Marketing Category NameANDA
Application NumberANDA091163
ManufacturerRising Pharma Holdings, Inc.
Substance NameFOSINOPRIL SODIUM
Strength40
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]

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