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"16714-221-01" National Drug Code (NDC)
Granisetron Hydrochloride 20 TABLET, FILM COATED in 1 BOTTLE (16714-221-01)
(Northstar Rx LLC)
NDC Code
16714-221-01
Package Description
20 TABLET, FILM COATED in 1 BOTTLE (16714-221-01)
Product NDC
16714-221
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Granisetron Hydrochloride
Non-Proprietary Name
Granisetron Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20080429
End Marketing Date
20210831
Marketing Category Name
ANDA
Application Number
ANDA078678
Manufacturer
Northstar Rx LLC
Substance Name
GRANISETRON HYDROCHLORIDE
Strength
1
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/16714-221-01