0009-0017 : Halcion 0.25 mg Oral Tablet


NDC0009-0017
Labeler: Pharmacia and Upjohn Company
Product Type: Human Prescription Drug
Drug Name:  Halcion
Dosage Form: Oral Tablet
Application #: NDA017892
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: HALCION;0;25
Shapes:  Oval
Colors:  Blue
Size (mm): 8
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:

  • 0009-0017-02: 500 TABLET IN 1 BOTTLE (0009‑0017‑02)
  • 0009-0017-55: 100 BLISTER PACK IN 1 CARTON (0009‑0017‑55) > 1 TABLET IN 1 BLISTER PACK
  • 0009-0017-58: 10 TABLET IN 1 BOTTLE (0009‑0017‑58)
  • 0009-0017-59: 10 BOTTLE IN 1 CARTON (0009‑0017‑59) > 10 TABLET IN 1 BOTTLE

Active Ingredients:

  • Triazolam

Dosage Strength:

  • .25 mg

Inactive Ingredients:

  • Powdered Cellulose
  • Starch, Corn
  • Docusate Sodium
  • Fd&c Blue No. 2
  • Lactose
  • Magnesium Stearate
  • Silicon Dioxide
  • Sodium Benzoate

Pharmaceutical Classes:

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

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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.