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"68071-3878-9" National Drug Code (NDC)

Labetalol Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (68071-3878-9)
(NuCare Pharmaceuticals , Inc.)

NDC Code68071-3878-9
Package Description90 TABLET, FILM COATED in 1 BOTTLE (68071-3878-9)
Product NDC68071-3878
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210527
Marketing Category NameANDA
Application NumberANDA209603
ManufacturerNuCare 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/68071-3878-9





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