"68788-7372-8" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BOTTLE (68788-7372-8)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7372-8
Package Description21 TABLET in 1 BOTTLE (68788-7372-8)
Product NDC68788-7372
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20170221
Marketing Category NameANDA
Application NumberANDA040362
ManufacturerPreferred Pharmaceuticals Inc.
Substance NamePREDNISONE
Strength5
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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