67386-313 : Onfi 2.5 mg/ml Oral Suspension
| NDC: | 67386-313 |
| Labeler: | Lundbeck LLC |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Onfi |
| Dosage Form: | Oral Suspension |
| Application #: | NDA203993 |
| 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:
- 67386-313-21: 1 BOTTLE IN 1 CARTON (67386‑313‑21) > 120 ML IN 1 BOTTLE
Active Ingredients:
- Clobazam
Dosage Strength:
- 2.5 mg/mL
Pharmaceutical Classes:
- Benzodiazepine [EPC]
- Benzodiazepines [CS]
- Cytochrome P450 2D6 Inhibitors [MoA]
- Cytochrome P450 3A4 Inducers [MoA]
Related Products:
Based on records with the same trade name.- 67386-310 Onfi 5 mg Oral Tablet by Lundbeck LLC
- 67386-311 Onfi 10 mg Oral Tablet by Lundbeck LLC
- 67386-312 Onfi 20 mg Oral Tablet by Lundbeck LLC
- 67386-314 Onfi 10 mg/1 Oral Tablet by Lundbeck LLC
- 67386-315 Onfi 20 mg/1 Oral Tablet by Lundbeck 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.