NDC 68788-9511

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 ID68788-9511_2262375a-a3f5-43d7-851d-f8da50587986
NDC68788-9511
Product TypeHuman Prescription Drug
Proprietary NameLorazepam
Generic NameLorazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2014-02-05
Marketing CategoryANDA / ANDA
Application NumberANDA078203
Labeler NamePreferred Pharmaceuticals, Inc.
Substance NameLORAZEPAM
Active Ingredient Strength1 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 68788-9511-8

120 TABLET in 1 BOTTLE (68788-9511-8)
Marketing Start Date2014-02-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-9511-9 [68788951109]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA078203
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-05
Marketing End Date2019-10-23

NDC 68788-9511-3 [68788951103]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA078203
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-05
Marketing End Date2019-10-23

NDC 68788-9511-8 [68788951108]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA078203
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-05
Marketing End Date2019-10-23

NDC 68788-9511-6 [68788951106]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA078203
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-05
Marketing End Date2019-10-23

NDC 68788-9511-5 [68788951105]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA078203
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-05
Marketing End Date2019-10-23

NDC 68788-9511-1 [68788951101]

Lorazepam TABLET
Marketing CategoryANDA
Application NumberANDA078203
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-05
Marketing End Date2019-10-23

Drug Details

Active Ingredients

IngredientStrength
LORAZEPAM1 mg/1

OpenFDA Data

SPL SET ID:5c6bb800-ad50-4e9f-a996-02405f7ea60a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 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

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