58151-504 : Xanax 1 mg Oral Tablet, Extended Release


NDC58151-504
Labeler: Viatris Specialty LLC
Product Type: Human Prescription Drug
Drug Name:  Xanax XR
Dosage Form: Oral Tablet, Extended Release
Application #: NDA021434
Rev. Date: 
CSA Schedule: CIV (US) [1]


[1] Schedule IV Controlled Substance: Low potential for abuse relative to substances in Schedule III. Examples include Alprazolam (Xanax), Diazepam (Valium), Carisoprodol (Soma), Clonazepam (Klonopin), Lorazepam (Ativan), Clorazepate (Tranxene), Midazolam (Versed), Temazepam (Restoril), and Triazolam (Halcion).. More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 58151-504-91: 60 TABLET, EXTENDED RELEASE IN 1 BOTTLE (58151‑504‑91)

Active Ingredients:

  • Alprazolam

Dosage Strength:

  • 1 mg

Pharmaceutical Classes:

  • Benzodiazepine [EPC]
  • Benzodiazepines [CS]

Related Products:

Based on records with the same trade name.
  • 58151-503 Xanax .5 mg Oral Tablet, Extended Release by Viatris Specialty LLC
  • 58151-505 Xanax 2 mg Oral Tablet, Extended Release by Viatris Specialty LLC
  • 58151-506 Xanax 3 mg Oral Tablet, Extended Release by Viatris Specialty LLC

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.