50474-870 : Briviact 10 mg/ml Oral Solution
| NDC: | 50474-870 |
| Labeler: | Ucb, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Briviact |
| Dosage Form: | Oral Solution |
| Application #: | NDA205838 |
| Rev. Date: | |
| CSA Schedule: | CV (US) [1] |
[1] Schedule V Controlled Substance: Low potential for abuse relative to substances listed in Schedule IV and consist primarily of preparations containing limited quantities of certain narcotics. (i.e. Cough preparations containing not more than 200 milligrams of Codeine per 100 milliliters or per 100 grams [such as Robitussin AC, Phenergan with Codeine], and Ezogabine). More Details: US Dept of Justice Controlled Substance Schedules.
NDC Package Codes:
- 50474-870-15: 1 BOTTLE IN 1 CARTON (50474‑870‑15) > 300 ML IN 1 BOTTLE
Active Ingredients:
- Brivaracetam
Dosage Strength:
- 10 mg/mL
Pharmaceutical Classes:
- Epoxide Hydrolase Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 50474-370 Briviact 10 mg Oral Tablet, Film Coated by Ucb, Inc.
- 50474-470 Briviact 25 mg Oral Tablet, Film Coated by Ucb, Inc.
- 50474-570 Briviact 50 mg Oral Tablet, Film Coated by Ucb, Inc.
- 50474-670 Briviact 75 mg Oral Tablet, Film Coated by Ucb, Inc.
- 50474-770 Briviact 100 mg Oral Tablet, Film Coated by Ucb, Inc.
- 50474-970 Briviact 50 mg/5ml Intravenous Injection, Suspension by Ucb, Inc.
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