"51991-838-10" National Drug Code (NDC)

Cyproheptadine Hydrochloride 1000 TABLET in 1 BOTTLE (51991-838-10)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-838-10
Package Description1000 TABLET in 1 BOTTLE (51991-838-10)
Product NDC51991-838
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyproheptadine Hydrochloride
Non-Proprietary NameCyproheptadine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20131021
End Marketing Date20240131
Marketing Category NameANDA
Application NumberANDA040644
ManufacturerBreckenridge Pharmaceutical, Inc.
Substance NameCYPROHEPTADINE HYDROCHLORIDE
Strength4
Strength Unitmg/1

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