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

"68001-205-03" National Drug Code (NDC)

Labetalol Hcl 500 TABLET, FILM COATED in 1 BOTTLE (68001-205-03)
(BluePoint Laboratories)

NDC Code68001-205-03
Package Description500 TABLET, FILM COATED in 1 BOTTLE (68001-205-03)
Product NDC68001-205
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hcl
Non-Proprietary NameLabetalol Hcl
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140226
End Marketing Date20210731
Marketing Category NameANDA
Application NumberANDA075113
ManufacturerBluePoint Laboratories
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68001-205-03





Copyright © 2007-2024 www.ndcvalidator.com