"61919-291-37" National Drug Code (NDC)

Prednisolone 240 mL in 1 BOTTLE (61919-291-37)
(DIRECT RX)

NDC Code61919-291-37
Package Description240 mL in 1 BOTTLE (61919-291-37)
Product NDC61919-291
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisolone
Non-Proprietary NamePrednisolone
Dosage FormSOLUTION
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA040401
ManufacturerDIRECT RX
Substance NamePREDNISOLONE
Strength15
Strength Unitmg/5mL
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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