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"70377-060-13" National Drug Code (NDC)
Labetalol Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (70377-060-13)
(Biocon Pharma Inc.)
NDC Code
70377-060-13
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (70377-060-13)
Product NDC
70377-060
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
20210527
Marketing Category Name
ANDA
Application Number
ANDA209603
Manufacturer
Biocon Pharma Inc.
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/70377-060-13