66869-564 : Seglentis Oral Tablet
| NDC: | 66869-564 |
| Labeler: | Kowa Pharmaceuticals America, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Seglentis |
| Dosage Form: | Oral Tablet |
| Application #: | NDA213426 |
| 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:
- 66869-564-30: 1 BOTTLE, PLASTIC IN 1 CARTON (66869‑564‑30) > 30 TABLET IN 1 BOTTLE, PLASTIC
- 66869-564-35: 35 TABLET IN 1 BOTTLE, PLASTIC (66869‑564‑35)
- 66869-564-90: 1 BOTTLE, PLASTIC IN 1 CARTON (66869‑564‑90) > 90 TABLET IN 1 BOTTLE, PLASTIC
Active Ingredients:
- Celecoxib
- Tramadol Hydrochloride
Dosage Strength:
- 56 mg
- 44 mg
Pharmaceutical Classes:
- Anti-Inflammatory Agents
- Non-Steroidal [CS]
- Cyclooxygenase Inhibitors [MoA]
- Full Opioid Agonists [MoA]
- Nonsteroidal Anti-inflammatory Drug [EPC]
- Opioid Agonist [EPC]
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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.