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"61919-342-21" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BOTTLE (61919-342-21)
(DirectRX)

NDC Code61919-342-21
Package Description21 TABLET in 1 BOTTLE (61919-342-21)
Product NDC61919-342
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20150101
Marketing Category NameANDA
Application NumberANDA083677
ManufacturerDirectRX
Substance NamePREDNISONE
Strength20
Strength Unitmg/1
Pharmacy ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-342-21





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