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"0781-1679-13" National Drug Code (NDC)
Ondansetron 10 BLISTER PACK in 1 CARTON (0781-1679-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Sandoz Inc)
NDC Code
0781-1679-13
Package Description
10 BLISTER PACK in 1 CARTON (0781-1679-13) > 10 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
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/0781-1679-13