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"0781-1679-33" National Drug Code (NDC)
Ondansetron 1 BLISTER PACK in 1 CARTON (0781-1679-33) > 3 TABLET, FILM COATED in 1 BLISTER PACK
(Sandoz Inc)
NDC Code
0781-1679-33
Package Description
1 BLISTER PACK in 1 CARTON (0781-1679-33) > 3 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
0781-1679
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ondansetron
Non-Proprietary Name
Ondansetron
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20070625
End Marketing Date
20191130
Marketing Category Name
ANDA
Application Number
ANDA077517
Manufacturer
Sandoz 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/0781-1679-33