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"51991-705-10" National Drug Code (NDC)

Alprazolam 1000 TABLET in 1 BOTTLE (51991-705-10)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-705-10
Package Description1000 TABLET in 1 BOTTLE (51991-705-10)
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

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51991-705-10





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