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"21695-835-30" National Drug Code (NDC)
Ondansetron Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (21695-835-30)
(Rebel Distributors Corp)
NDC Code
21695-835-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (21695-835-30)
Product NDC
21695-835
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
20070625
Marketing Category Name
ANDA
Application Number
ANDA077050
Manufacturer
Rebel Distributors Corp
Substance Name
ONDANSETRON HYDROCHLORIDE
Strength
8
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/21695-835-30