NDC 52817-292

Oxazepam

Oxazepam

Oxazepam is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Trupharma, Llc. The primary component is Oxazepam.

Product ID52817-292_0bb751ed-e01b-4fe6-bde4-511bfd3aebbc
NDC52817-292
Product TypeHuman Prescription Drug
Proprietary NameOxazepam
Generic NameOxazepam
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2020-03-19
Marketing CategoryANDA / ANDA
Application NumberANDA071026
Labeler NameTruPharma, LLC
Substance NameOXAZEPAM
Active Ingredient Strength30 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 52817-292-10

100 CAPSULE in 1 BOTTLE (52817-292-10)
Marketing Start Date2020-03-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52817-292-10 [52817029210]

Oxazepam CAPSULE
Marketing CategoryANDA
Application NumberANDA071026
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-03-19

Drug Details

Active Ingredients

IngredientStrength
OXAZEPAM30 mg/1

OpenFDA Data

SPL SET ID:bda8bc70-3328-46f2-89d5-7ef7a061b418
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198057
  • 312134
  • 198059
  • UPC Code
  • 0352817292100
  • 0352817291103
  • 0352817290106
  • Pharmacological Class

    • Benzodiazepine [EPC]
    • Benzodiazepines [CS]

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

    NDCBrand NameGeneric Name
    0228-2067OxazepamOxazepam
    0228-2069OxazepamOxazepam
    0228-2073OxazepamOxazepam
    0781-2809OxazepamOxazepam
    0781-2810OxazepamOxazepam
    0781-2811OxazepamOxazepam
    43353-074OxazepamOxazepam
    43353-965OxazepamOxazepam
    43353-980OxazepamOxazepam
    52817-290OxazepamOxazepam
    52817-291OxazepamOxazepam
    52817-292OxazepamOxazepam
    62584-812OxazepamOxazepam
    62584-813OxazepamOxazepam
    62584-814OxazepamOxazepam
    67544-294OxazepamOxazepam
    67544-117OxazepamOxazepam
    67544-268OxazepamOxazepam

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