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"69292-502-10" National Drug Code (NDC)
Labetalol Hydrochloride 100 TABLET, COATED in 1 BOTTLE (69292-502-10)
(AMICI PHARMACEUTICALS LLC)
NDC Code
69292-502-10
Package Description
100 TABLET, COATED in 1 BOTTLE (69292-502-10)
Product NDC
69292-502
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Labetalol Hydrochloride
Non-Proprietary Name
Labetalol Hydrochloride
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20180501
Marketing Category Name
ANDA
Application Number
ANDA075215
Manufacturer
AMICI PHARMACEUTICALS LLC
Substance Name
LABETALOL
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/69292-502-10