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"21695-834-12" National Drug Code (NDC)

Ondansetron Hydrochloride 12 TABLET, FILM COATED in 1 BOTTLE (21695-834-12)
(Rebel Distributors Corp)

NDC Code21695-834-12
Package Description12 TABLET, FILM COATED in 1 BOTTLE (21695-834-12)
Product NDC21695-834
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron Hydrochloride
Non-Proprietary NameOndansetron Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070625
Marketing Category NameANDA
Application NumberANDA077050
ManufacturerRebel Distributors Corp
Substance NameONDANSETRON HYDROCHLORIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/21695-834-12





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