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"70518-3622-1" National Drug Code (NDC)

Methylprednisolone 21 TABLET in 1 BOTTLE, PLASTIC (70518-3622-1)
(REMEDYREPACK INC.)

NDC Code70518-3622-1
Package Description21 TABLET in 1 BOTTLE, PLASTIC (70518-3622-1)
Product NDC70518-3622
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethylprednisolone
Non-Proprietary NameMethylprednisolone
Dosage FormTABLET
UsageORAL
Start Marketing Date20230125
Marketing Category NameANDA
Application NumberANDA206751
ManufacturerREMEDYREPACK INC.
Substance NameMETHYLPREDNISOLONE
Strength4
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3622-1





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