"17856-0759-6" National Drug Code (NDC)

Prednisolone Sodium Phosphate 1 BOX in 1 CUP, UNIT-DOSE (17856-0759-6) / 72 CUP, UNIT-DOSE in 1 BOX (17856-0759-2) / 10 mL in 1 CUP, UNIT-DOSE
(ATLANTIC BIOLOGICALS CORP.)

NDC Code17856-0759-6
Package Description1 BOX in 1 CUP, UNIT-DOSE (17856-0759-6) / 72 CUP, UNIT-DOSE in 1 BOX (17856-0759-2) / 10 mL in 1 CUP, UNIT-DOSE
Product NDC17856-0759
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisolone Sodium Phosphate
Non-Proprietary NamePrednisolone Sodium Phosphate
Dosage FormSOLUTION
UsageORAL
Start Marketing Date20050425
Marketing Category NameANDA
Application NumberANDA076913
ManufacturerATLANTIC BIOLOGICALS CORP.
Substance NamePREDNISOLONE SODIUM PHOSPHATE
Strength15
Strength Unitmg/5mL
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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