"68001-005-01" National Drug Code (NDC)

Methylprednisolone 21 TABLET in 1 BLISTER PACK (68001-005-01)
(BluePoint Laboratories)

NDC Code68001-005-01
Package Description21 TABLET in 1 BLISTER PACK (68001-005-01)
Product NDC68001-005
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethylprednisolone
Non-Proprietary NameMethylprednisolone
Dosage FormTABLET
UsageORAL
Start Marketing Date20130802
Marketing Category NameANDA
Application NumberANDA040189
ManufacturerBluePoint Laboratories
Substance NameMETHYLPREDNISOLONE
Strength4
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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