"70095-043-30" National Drug Code (NDC)

Deflazacort 1 BOTTLE in 1 CARTON (70095-043-30) / 30 TABLET in 1 BOTTLE
(Sun Pharmaceutical Industries Limited)

NDC Code70095-043-30
Package Description1 BOTTLE in 1 CARTON (70095-043-30) / 30 TABLET in 1 BOTTLE
Product NDC70095-043
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDeflazacort
Non-Proprietary NameDeflazacort
Dosage FormTABLET
UsageORAL
Start Marketing Date20250319
Marketing Category NameANDA
Application NumberANDA217741
ManufacturerSun Pharmaceutical Industries Limited
Substance NameDEFLAZACORT
Strength36
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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