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"53808-1121-1" National Drug Code (NDC)
Ondansetron Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-1121-1)
(DOH CENTRAL PHARMACY)
NDC Code
53808-1121-1
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (53808-1121-1)
Product NDC
53808-1121
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
20170914
Marketing Category Name
ANDA
Application Number
ANDA078539
Manufacturer
DOH CENTRAL PHARMACY
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/53808-1121-1