"51991-704-05" National Drug Code (NDC)

Alprazolam 500 TABLET in 1 BOTTLE (51991-704-05)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-704-05
Package Description500 TABLET in 1 BOTTLE (51991-704-05)
Product NDC51991-704
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.25
Strength Unitmg/1
Pharmacy ClassesBenzodiazepine [EPC], Benzodiazepines [CS]
DEA ScheduleCIV

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