"16571-805-10" National Drug Code (NDC)

Cyproheptadine Hydrochloride 1000 TABLET in 1 BOTTLE (16571-805-10)
(Rising Pharma Holdings, Inc.)

NDC Code16571-805-10
Package Description1000 TABLET in 1 BOTTLE (16571-805-10)
Product NDC16571-805
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyproheptadine Hydrochloride
Non-Proprietary NameCyproheptadine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20220209
Marketing Category NameANDA
Application NumberANDA207555
ManufacturerRising Pharma Holdings, Inc.
Substance NameCYPROHEPTADINE HYDROCHLORIDE
Strength4
Strength Unitmg/1

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