NDC 71993-265

Quazepam

Quazepam

Quazepam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Atland Pharmaceuticals, Llc. The primary component is Quazepam.

Product ID71993-265_18eb814a-d169-43c2-991d-297fc2c52918
NDC71993-265
Product TypeHuman Prescription Drug
Proprietary NameQuazepam
Generic NameQuazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-03-20
Marketing CategoryNDA / NDA
Application NumberNDA018708
Labeler NameAtland Pharmaceuticals, LLC
Substance NameQUAZEPAM
Active Ingredient Strength15 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71993-265-10

100 TABLET in 1 BOTTLE (71993-265-10)
Marketing Start Date2018-03-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71993-265-30 [71993026530]

Quazepam TABLET
Marketing CategoryNDA
Application NumberNDA018708
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-03-20

NDC 71993-265-10 [71993026510]

Quazepam TABLET
Marketing CategoryNDA
Application NumberNDA018708
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-03-20

Drug Details

Active Ingredients

IngredientStrength
QUAZEPAM15 mg/1

OpenFDA Data

SPL SET ID:f7d63f3f-5303-48ab-bce2-35fd62c45799
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198183
  • UPC Code
  • 0371993265104
  • Pharmacological Class

    • Benzodiazepine [EPC]
    • Benzodiazepines [CS]

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

    NDCBrand NameGeneric Name
    50090-1474QuazepamQUAZEPAM
    71993-265QuazepamQuazepam
    61825-165DoralQuazepam

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