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"68682-309-30" National Drug Code (NDC)

Budesonide 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-309-30)
(Oceanside Pharmaceuticals)

NDC Code68682-309-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-309-30)
Product NDC68682-309
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBudesonide
Non-Proprietary NameBudesonide
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180710
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA203634
ManufacturerOceanside Pharmaceuticals
Substance NameBUDESONIDE
Strength9
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68682-309-30





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