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"71209-083-10" National Drug Code (NDC)
Labetalol Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (71209-083-10)
(Cadila Pharmaceuticals Limited)
NDC Code
71209-083-10
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (71209-083-10)
Product NDC
71209-083
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Labetalol Hydrochloride
Non-Proprietary Name
Labetalol Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20180529
Marketing Category Name
ANDA
Application Number
ANDA211325
Manufacturer
Cadila Pharmaceuticals Limited
Substance Name
LABETALOL HYDROCHLORIDE
Strength
100
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/71209-083-10