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"70518-4145-0" National Drug Code (NDC)
Ondansetron Hydrochloride 16 TABLET, FILM COATED in 1 BLISTER PACK (70518-4145-0)
(REMEDYREPACK INC.)
NDC Code
70518-4145-0
Package Description
16 TABLET, FILM COATED in 1 BLISTER PACK (70518-4145-0)
Product NDC
70518-4145
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ondansetron Hydrochloride
Non-Proprietary Name
Ondansetron Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20240718
Marketing Category Name
ANDA
Application Number
ANDA078539
Manufacturer
REMEDYREPACK INC.
Substance Name
ONDANSETRON HYDROCHLORIDE
Strength
4
Strength Unit
mg/1
Pharmacy Classes
Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-4145-0