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"71930-036-12" National Drug Code (NDC)
Labetalol Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (71930-036-12)
(Eywa Pharma Inc)
NDC Code
71930-036-12
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (71930-036-12)
Product NDC
71930-036
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
20190524
Marketing Category Name
ANDA
Application Number
ANDA207863
Manufacturer
Eywa Pharma Inc
Substance Name
LABETALOL HYDROCHLORIDE
Strength
200
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/71930-036-12