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"51672-4042-2" National Drug Code (NDC)

Clorazepate Dipotassium 500 TABLET in 1 BOTTLE (51672-4042-2)
(Taro Pharmaceuticals U.S.A., Inc.)

NDC Code51672-4042-2
Package Description500 TABLET in 1 BOTTLE (51672-4042-2)
Product NDC51672-4042
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameClorazepate Dipotassium
Non-Proprietary NameClorazepate Dipotassium
Dosage FormTABLET
UsageORAL
Start Marketing Date20000427
Marketing Category NameANDA
Application NumberANDA075731
ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Substance NameCLORAZEPATE DIPOTASSIUM
Strength3.75
Strength Unitmg/1
Pharmacy ClassesBenzodiazepine [EPC], Benzodiazepines [CS]
DEA ScheduleCIV

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-4042-2





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