www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"70518-2903-0" National Drug Code (NDC)

Labetalol Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2903-0)
(REMEDYREPACK INC.)

NDC Code70518-2903-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2903-0)
Product NDC70518-2903
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20201008
Marketing Category NameANDA
Application NumberANDA207863
ManufacturerREMEDYREPACK INC.
Substance NameLABETALOL HYDROCHLORIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2903-0





Copyright © 2007-2024 www.ndcvalidator.com