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"24979-169-06" National Drug Code (NDC)

Labetalol Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (24979-169-06)
(TWi Pharmaceuticals, Inc.)

NDC Code24979-169-06
Package Description30 TABLET, FILM COATED in 1 BOTTLE (24979-169-06)
Product NDC24979-169
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180801
Marketing Category NameANDA
Application NumberANDA209603
ManufacturerTWi Pharmaceuticals, 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/24979-169-06





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