"13107-282-05" National Drug Code (NDC)

Clorazepate Dipotassium 500 TABLET in 1 BOTTLE, PLASTIC (13107-282-05)
(Aurolife Pharma LLC)

NDC Code13107-282-05
Package Description500 TABLET in 1 BOTTLE, PLASTIC (13107-282-05)
Product NDC13107-282
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameClorazepate Dipotassium
Non-Proprietary NameClorazepate Dipotassium
Dosage FormTABLET
UsageORAL
Start Marketing Date20230923
Marketing Category NameANDA
Application NumberANDA071858
ManufacturerAurolife Pharma LLC
Substance NameCLORAZEPATE DIPOTASSIUM
Strength3.75
Strength Unitmg/1
Pharmacy ClassesBenzodiazepine [EPC], Benzodiazepines [CS]
DEA ScheduleCIV

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