59762-3717 : Triazolam 0.125 mg Oral Tablet
NDC: | 59762-3717 |
Labeler: | Greenstone LLC |
Product Type: | Human Prescription Drug |
Drug Name: | Triazolam |
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: | G3717 |
Shapes: |
Oval |
Colors: |
White |
Size (mm): | 8 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 59762-3717-4: 10 BOTTLE IN 1 PACKAGE (59762‑3717‑4) > 10 TABLET IN 1 BOTTLE
- 59762-3717-9: 100 TABLET IN 1 BOTTLE (59762‑3717‑9)
Active Ingredients:
- Triazolam
Dosage Strength:
- .125 mg
Inactive Ingredients:
- Powdered Cellulose
- Starch, Corn
- Docusate Sodium
- Lactose
- Magnesium Stearate
- Silicon Dioxide
- Sodium Benzoate
Pharmaceutical Classes:
- Benzodiazepine [EPC]
- Benzodiazepines [CS]
Related Products:
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NDC 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.