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"71335-0118-4" National Drug Code (NDC)
Labetalol Hydrochloride 90 TABLET in 1 BOTTLE (71335-0118-4)
(Bryant Ranch Prepack)
NDC Code
71335-0118-4
Package Description
90 TABLET in 1 BOTTLE (71335-0118-4)
Product NDC
71335-0118
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Labetalol Hydrochloride
Non-Proprietary Name
Labetalol Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20141201
Marketing Category Name
NDA
Application Number
NDA018716
Manufacturer
Bryant Ranch Prepack
Substance Name
LABETALOL HYDROCHLORIDE
Strength
300
Strength Unit
mg/1
Pharmacy Classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0118-4