0051-4390 : Clorazepate Dipotassium T-tab 7.5 mg Oral Tablet


NDC0051-4390
Labeler: Abbvie Inc.
Product Type: Human Prescription Drug
Drug Name:  Clorazepate Dipotassium T-tab
Dosage Form: Oral Tablet
Application #: NDA017105
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.

Appearance:


Markings: T;OV;32
Shapes:  Freeform
Colors:  Orange
Size (mm): 9
Segments: * 2

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

NDC Package Codes:

  • 0051-4390-13: 100 TABLET IN 1 BOTTLE (0051‑4390‑13)

Active Ingredients:

  • Clorazepate Dipotassium

Dosage Strength:

  • 7.5 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Fd&c Yellow No. 6
  • Magnesium Oxide
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Potassium Carbonate
  • Potassium Chloride
  • Talc

Pharmaceutical Classes:

  • Benzodiazepine [EPC]
  • Benzodiazepines [Chemical/Ingredient]

NDC QR Code

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NDC 0051-4390 QR Code

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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.