"42708-177-21" National Drug Code (NDC)

Cyproheptadine Hydrochloride 21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)
(QPharma Inc)

NDC Code42708-177-21
Package Description21 TABLET in 1 BOTTLE, PLASTIC (42708-177-21)
Product NDC42708-177
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyproheptadine Hydrochloride
Non-Proprietary NameCyproheptadine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20170117
Marketing Category NameANDA
Application NumberANDA206553
ManufacturerQPharma Inc
Substance NameCYPROHEPTADINE HYDROCHLORIDE
Strength4
Strength Unitmg/1

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