NDC 33261-005

Alprazolam

Alprazolam

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

Product ID33261-005_93729350-108f-4474-811d-9e4ca0294eac
NDC33261-005
Product TypeHuman Prescription Drug
Proprietary NameAlprazolam
Generic NameAlprazolam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2007-03-28
Marketing CategoryANDA / ANDA
Application NumberANDA074174
Labeler NameAidarex Pharmaceuticals LLC
Substance NameALPRAZOLAM
Active Ingredient Strength1 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 33261-005-30

30 TABLET in 1 BOTTLE, PLASTIC (33261-005-30)
Marketing Start Date2007-03-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 33261-005-42 [33261000542]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-03-28
Inactivation Date2020-01-31

NDC 33261-005-15 [33261000515]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-28
Inactivation Date2020-01-31

NDC 33261-005-10 [33261000510]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-03-28
Inactivation Date2020-01-31

NDC 33261-005-00 [33261000500]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-28
Inactivation Date2020-01-31

NDC 33261-005-45 [33261000545]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-03-28
Inactivation Date2020-01-31

NDC 33261-005-60 [33261000560]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-28
Inactivation Date2020-01-31

NDC 33261-005-90 [33261000590]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-28
Inactivation Date2020-01-31

NDC 33261-005-30 [33261000530]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-28
Inactivation Date2020-01-31

NDC 33261-005-02 [33261000502]

Alprazolam TABLET
Marketing CategoryANDA
Application NumberANDA074174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-03-28
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALPRAZOLAM1 mg/1

OpenFDA Data

SPL SET ID:fd3d0e37-470d-4216-8070-24a206930eac
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197321
  • 197322
  • 308048
  • 308047

    • Pharmacological Class

    • Benzodiazepine [EPC]
    • Benzodiazepines [CS]

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

    NDCBrand NameGeneric Name
    0054-3068AlprazolamAlprazolam
    0228-2027AlprazolamAlprazolam
    68071-3049AlprazolamAlprazolam
    68071-1966AlprazolamAlprazolam
    68071-1888AlprazolamAlprazolam
    68071-1884AlprazolamAlprazolam
    68071-1929AlprazolamAlprazolam
    68071-4621AlprazolamAlprazolam
    68071-4447AlprazolamAlprazolam
    68071-4818AlprazolamAlprazolam
    68071-4831AlprazolamAlprazolam
    68071-4652AlprazolamAlprazolam
    68084-672AlprazolamAlprazolam
    68084-647AlprazolamAlprazolam
    68788-6865AlprazolamAlprazolam
    68788-0575AlprazolamAlprazolam
    68788-2029AlprazolamAlprazolam
    68788-6381AlprazolamAlprazolam
    68788-6358AlprazolamAlprazolam
    68788-2027AlprazolamAlprazolam
    68788-9430AlprazolamAlprazolam
    68788-9727AlprazolamAlprazolam
    68788-9997AlprazolamAlprazolam
    68788-9682AlprazolamAlprazolam
    70518-0000AlprazolamAlprazolam
    70518-0966AlprazolamAlprazolam
    71205-227AlprazolamAlprazolam
    71335-0163AlprazolamAlprazolam
    71335-0098AlprazolamAlprazolam
    71335-0247AlprazolamAlprazolam
    71335-0215AlprazolamAlprazolam
    71335-0252AlprazolamAlprazolam
    71335-0448AlprazolamAlprazolam
    71335-0673AlprazolamAlprazolam
    71335-0680AlprazolamAlprazolam
    71335-0761AlprazolamAlprazolam
    71335-0422AlprazolamAlprazolam
    71335-0850AlprazolamAlprazolam
    71335-0929AlprazolamAlprazolam
    71335-0813AlprazolamAlprazolam
    71335-0849AlprazolamAlprazolam
    71610-113AlprazolamAlprazolam
    71335-0920AlprazolamAlprazolam
    71610-112AlprazolamAlprazolam
    75921-901ALPRAZOLAMALPRAZOLAM
    0615-7794AlprazolamAlprazolam
    0615-7795AlprazolamAlprazolam
    0615-7793AlprazolamAlprazolam
    0615-7999AlprazolamAlprazolam
    0615-8000AlprazolamAlprazolam
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.