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"68382-799-16" National Drug Code (NDC)

Labetalol Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (68382-799-16)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-799-16
Package Description90 TABLET, FILM COATED in 1 BOTTLE (68382-799-16)
Product NDC68382-799
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171205
Marketing Category NameANDA
Application NumberANDA207743
ManufacturerZydus Pharmaceuticals USA 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/68382-799-16





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