Brivaracetam 10 MG/ML Oral Solution [Briviact] — RxCUI 1739788
RxNorm drug concept · Semantic branded drug
RxCUI 1739788
Semantic branded drug · SBD
● Current RxNorm concept 7 FDA products
13 package NDCs
Snapshot Jul 14, 2026
What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.
🗂️ Key Facts
RxCUI1739788
Official nameBrivaracetam 10 MG/ML Oral Solution [Briviact]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asBriviact 10 MG per 1 ML Oral Solution; BRIVIACT 10 MG in 1 mL Oral Solution
FDA products mapped7
Package NDCs mapped13
Reported Medicaid activity (SDUD)174,041 prescriptions · 52 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Brivaracetam Injection: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Briviact injection is used when you temporarily can't swallow tablets or liquid — for example, if you're in the hospital, recovering from a procedure, or having trouble swallowing....
- Why am I getting brivaracetam as an injection instead of a pill?
- The most common ones are drowsiness, dizziness, fatigue, and nausea. These tend to be most noticeable early in treatment. Most people manage them fine, but you should avoid driving...
- What side effects are most common and should I be worried about them?
🕸️ Concept Web — How Brivaracetam 10 MG/ML Oral Solution [Briviact] Connects
One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept
Brivaracetam 10 MG/ML Oral Solution [Briviact]
RxCUI 1739788 Semantic branded drug · SBD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 1
The active substance itself — no strength, form, or brand attached yet.
-
Brivaracetam
1739745IN
-
Brivaracetam
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Briviact
1739750BN
-
Briviact
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Brivaracetam Oral Solution
1739784SCDF -
Brivaracetam Oral Liquid Product
1739783SCDG -
Brivaracetam Oral Product
1739758SCDG -
Brivaracetam Oral Solution [Briviact]
1739786SBDF -
Briviact Oral Liquid Product
1739787SBDG -
Briviact Oral Product
1739764SBDG -
Oral Solution
316968DF -
Oral Liquid Product
1151137DFG - +1 more in this family
-
Brivaracetam Oral Solution
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Brivaracetam 10 MG/ML Oral Solution
1739785SCD -
Brivaracetam 10 MG/ML
1739746SCDC -
Brivaracetam 10 MG/ML [Briviact]
1739751SBDC
-
Brivaracetam 10 MG/ML Oral Solution
Showing up to 8 concepts per family — 13 of 14 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.
🔀 Generic ⇄ Brand Crosswalk
The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.
Generic (Clinical) Concepts
-
Brivaracetam 10 MG/ML Oral Solution
SCD · 1739785 -
Brivaracetam 10 MG/ML
SCDC · 1739746 -
Brivaracetam Oral Solution
SCDF · 1739784 -
Brivaracetam Oral Liquid Product
SCDG · 1739783 -
Brivaracetam Oral Product
SCDG · 1739758
Brand-Name Concepts
-
Brivaracetam 10 MG/ML [Briviact]
SBDC · 1739751 -
Brivaracetam Oral Solution [Briviact]
SBDF · 1739786 -
Briviact Oral Liquid Product
SBDG · 1739787 -
Briviact Oral Product
SBDG · 1739764 -
Briviact
BN · 1739750
📦 FDA Products & Package NDCs
7 products · 13 package NDCs
13 package NDCs map to RxCUI 1739788 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
| Package NDC | Package | Brand / generic name | Labeler | Marketing start |
|---|---|---|---|---|
| 50474-0370-66 | 1 BOTTLE in 1 CARTON (50474-370-66) / 60 TABLET, FILM COATE... | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0470-09 | 100 BLISTER PACK in 1 CARTON (50474-470-09) / 1 TABLET, FIL... | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0470-14 | 1 BLISTER PACK in 1 CARTON (50474-470-14) / 14 TABLET, FILM... | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0470-66 | 1 BOTTLE in 1 CARTON (50474-470-66) / 60 TABLET, FILM COATE... | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0570-09 | 100 BLISTER PACK in 1 CARTON (50474-570-09) / 1 TABLET, FIL... | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0570-14 | 1 BLISTER PACK in 1 CARTON (50474-570-14) / 14 TABLET, FILM... | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0570-66 | 1 BOTTLE in 1 CARTON (50474-570-66) / 60 TABLET, FILM COATE... | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0670-66 | 1 BOTTLE in 1 CARTON (50474-670-66) / 60 TABLET, FILM COATE... | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0770-09 | 100 BLISTER PACK in 1 CARTON (50474-770-09) / 1 TABLET, FIL... | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0770-14 | 1 BLISTER PACK in 1 CARTON (50474-770-14) / 14 TABLET, FILM... | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0770-66 | 1 BOTTLE in 1 CARTON (50474-770-66) / 60 TABLET, FILM COATE... | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0870-15 | 1 BOTTLE in 1 CARTON (50474-870-15) / 300 mL in 1 BOTTLE | Briviact | UCB, Inc. | 2016-05-12 |
| 50474-0970-75 | 10 VIAL, GLASS in 1 CARTON (50474-970-75) / 5 mL in 1 VIAL,... | Briviact | UCB, Inc. | 2016-05-12 |
Observed labelers:
UCB, Inc. (13)
— this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.
🗃️ Sources & Limits
Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
- A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
- Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
- Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
- Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.