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"70771-1163-1" National Drug Code (NDC)
Labetalol Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (70771-1163-1)
(Zydus Lifesciences Limited)
NDC Code
70771-1163-1
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (70771-1163-1)
Product NDC
70771-1163
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
20171205
Marketing Category Name
ANDA
Application Number
ANDA207743
Manufacturer
Zydus Lifesciences 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/70771-1163-1