NDC 71335-0806

Lorazepam

Lorazepam

Lorazepam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Lorazepam.

Product ID71335-0806_08ecce86-8f45-4c42-8f1e-112dcef0ee5e
NDC71335-0806
Product TypeHuman Prescription Drug
Proprietary NameLorazepam
Generic NameLorazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2007-01-03
Marketing CategoryANDA / ANDA
Application NumberANDA071403
Labeler NameBryant Ranch Prepack
Substance NameLORAZEPAM
Active Ingredient Strength1 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71335-0806-7

120 TABLET in 1 BOTTLE (71335-0806-7)
Marketing Start Date2015-10-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0806-3 [71335080603]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA071403
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-27
Marketing End Date2019-06-30

NDC 71335-0806-5 [71335080605]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA071403
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-27
Marketing End Date2019-06-30

NDC 71335-0806-1 [71335080601]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA071403
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-27
Marketing End Date2019-06-30

NDC 71335-0806-2 [71335080602]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA071403
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-27
Marketing End Date2019-06-30

NDC 71335-0806-8 [71335080608]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA071403
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-27
Marketing End Date2019-06-30

NDC 71335-0806-7 [71335080607]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA071403
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-27
Marketing End Date2019-06-30

NDC 71335-0806-4 [71335080604]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA071403
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-27
Marketing End Date2019-06-30

NDC 71335-0806-6 [71335080606]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA071403
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-27
Marketing End Date2019-06-30

Drug Details

Active Ingredients

IngredientStrength
LORAZEPAM.5 mg/1

OpenFDA Data

SPL SET ID:4fb48d28-bf60-4939-9756-c1da7ebb5379
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197900
  • 197901
  • 197902
  • Pharmacological Class

    • Benzodiazepine [EPC]
    • Benzodiazepines [CS]

    NDC Crossover Matching brand name "Lorazepam" or generic name "Lorazepam"

    NDCBrand NameGeneric Name
    0054-3532LorazepamLorazepam
    0093-3425LorazepamLorazepam
    0093-3426LorazepamLorazepam
    0093-3427LorazepamLorazepam
    0121-0770LorazepamLorazepam
    67544-982LorazepamLorazepam
    0409-6779LorazepamLorazepam
    0409-6778LorazepamLorazepam
    0409-6780LorazepamLorazepam
    68071-3010LorazepamLorazepam
    68071-3227LorazepamLorazepam
    68071-3121LorazepamLorazepam
    68071-3242LorazepamLorazepam
    68071-3096LorazepamLorazepam
    68084-736LorazepamLorazepam
    68084-742LorazepamLorazepam
    68084-754LorazepamLorazepam
    68788-0241LorazepamLorazepam
    68788-9511LorazepamLorazepam
    68788-7355LorazepamLorazepam
    68788-7411LorazepamLorazepam
    68788-9839LorazepamLorazepam
    68788-9258LorazepamLorazepam
    68788-9840LorazepamLorazepam
    68788-9982LorazepamLorazepam
    69315-904LorazepamLorazepam
    69315-906LorazepamLorazepam
    69315-905LorazepamLorazepam
    0591-0240LorazepamLorazepam
    0591-0241LorazepamLorazepam
    0591-0242LorazepamLorazepam
    70518-0155LorazepamLorazepam
    70518-0486LorazepamLorazepam
    70518-0275LorazepamLorazepam
    70518-0156LorazepamLorazepam
    70518-0445LorazepamLorazepam
    70518-1045LorazepamLorazepam
    70518-1431LorazepamLorazepam
    70518-1520LorazepamLorazepam
    70518-1313LorazepamLorazepam
    70518-1679LorazepamLorazepam
    70518-1255LorazepamLorazepam
    0603-4246LorazepamLorazepam
    71205-200LorazepamLorazepam
    71205-235LorazepamLorazepam
    71205-228LorazepamLorazepam
    71205-166LorazepamLorazepam
    71335-0277LorazepamLorazepam
    71335-0655LorazepamLorazepam
    71335-0204LorazepamLorazepam

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.