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"67046-1042-3" National Drug Code (NDC)
Labetalol Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1042-3)
(Coupler LLC)
NDC Code
67046-1042-3
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1042-3)
Product NDC
67046-1042
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
20241108
Marketing Category Name
ANDA
Application Number
ANDA207743
Manufacturer
Coupler LLC
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/67046-1042-3