"16714-221-30" National Drug Code (NDC)

Granisetron Hydrochloride 2 BLISTER PACK in 1 CARTON (16714-221-30) > 1 TABLET, FILM COATED in 1 BLISTER PACK (16714-221-10)
(Northstar Rx LLC)

NDC Code16714-221-30
Package Description2 BLISTER PACK in 1 CARTON (16714-221-30) > 1 TABLET, FILM COATED in 1 BLISTER PACK (16714-221-10)
Product NDC16714-221
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGranisetron Hydrochloride
Non-Proprietary NameGranisetron Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20080429
End Marketing Date20210831
Marketing Category NameANDA
Application NumberANDA078678
ManufacturerNorthstar Rx LLC
Substance NameGRANISETRON HYDROCHLORIDE
Strength1
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

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