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"68071-3180-3" National Drug Code (NDC)
Labetalol Hydrochloride 30 TABLET in 1 BOTTLE (68071-3180-3)
(NuCare Pharmaceuticals, Inc.)
NDC Code
68071-3180-3
Package Description
30 TABLET in 1 BOTTLE (68071-3180-3)
Product NDC
68071-3180
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Labetalol Hydrochloride
Non-Proprietary Name
Labetalol Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20141201
Marketing Category Name
NDA
Application Number
NDA018716
Manufacturer
NuCare Pharmaceuticals, 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/68071-3180-3