"67046-1029-3" National Drug Code (NDC)

Ondansetron Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1029-3)
(Coupler LLC)

NDC Code67046-1029-3
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1029-3)
Product NDC67046-1029
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOndansetron Hydrochloride
Non-Proprietary NameOndansetron Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20241111
Marketing Category NameANDA
Application NumberANDA078539
ManufacturerCoupler LLC
Substance NameONDANSETRON HYDROCHLORIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]

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