"51991-705-01" National Drug Code (NDC)

Alprazolam 100 TABLET in 1 BOTTLE (51991-705-01)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-705-01
Package Description100 TABLET in 1 BOTTLE (51991-705-01)
Product NDC51991-705
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAlprazolam
Non-Proprietary NameAlprazolam
Dosage FormTABLET
UsageORAL
Start Marketing Date20180709
End Marketing Date20251031
Marketing Category NameANDA
Application NumberANDA207507
ManufacturerBreckenridge Pharmaceutical, Inc.
Substance NameALPRAZOLAM
Strength.5
Strength Unitmg/1
Pharmacy ClassesBenzodiazepine [EPC], Benzodiazepines [CS]
DEA ScheduleCIV

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