NDC 68788-9839

Lorazepam

Lorazepam

Lorazepam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals, Inc. The primary component is Lorazepam.

Product ID68788-9839_4a06a04d-855f-4ec4-b1a3-17e50365bcf6
NDC68788-9839
Product TypeHuman Prescription Drug
Proprietary NameLorazepam
Generic NameLorazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2012-03-29
Marketing CategoryANDA / ANDA
Application NumberANDA076045
Labeler NamePreferred Pharmaceuticals, Inc
Substance NameLORAZEPAM
Active Ingredient Strength1 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 68788-9839-3

30 TABLET in 1 BOTTLE (68788-9839-3)
Marketing Start Date2012-03-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-9839-8 [68788983908]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA076045
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-03-29
Marketing End Date2019-10-23

NDC 68788-9839-9 [68788983909]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA076045
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-03-29
Marketing End Date2019-10-23

NDC 68788-9839-3 [68788983903]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA076045
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-03-29
Marketing End Date2019-10-23

NDC 68788-9839-6 [68788983906]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA076045
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-03-29
Marketing End Date2019-10-23

NDC 68788-9839-1 [68788983901]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA076045
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-03-29
Marketing End Date2019-10-23

Drug Details

Active Ingredients

IngredientStrength
LORAZEPAM1 mg/1

OpenFDA Data

SPL SET ID:85efece9-04fe-4b58-8340-6fd7208cfe85
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197900
  • 197901
  • 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.