62856-584 : Banzel 40 mg/ml Oral Suspension
NDC: | 62856-584 |
Labeler: | Eisai Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Banzel |
Dosage Form: | Oral Suspension |
Application #: | NDA201367 |
Rev. Date: |
NDC Package Codes:
- 62856-584-46: 1 BOTTLE IN 1 CARTON (62856‑584‑46) > 460 ML IN 1 BOTTLE
Active Ingredients:
- Rufinamide
Dosage Strength:
- 40 mg/mL
Related Products:
Based on records with the same trade name.- 62856-582 Banzel 200 mg Oral Tablet by Eisai Inc.
- 62856-583 Banzel 400 mg Oral Tablet by Eisai Inc.
- 68180-797 Banzel 40 mg/ml Oral Suspension by Lupin Pharmaceuticals, Inc.
- 75929-098 Banzel 400 mg Oral Tablet, Film Coated by Pharma Packaging Solutions, LLC Dba Tjoapack LLC
NDC QR Code
Scan the QR code below to easily reference this data in the future:< Prev: 62856-583Next: 62856-600 >
Related Discussions:
Anyone have experience with banzel?
My son is on banzel(along with 280ml of phenobarbital and1200 of keppra)for seizures. He's non verbal so he can'... 1 reply
My son is on banzel(along with 280ml of phenobarbital and1200 of keppra)for seizures. He's non verbal so he can'... 1 reply
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.