brivaracetam
- Product NDC
- 72205-269
- 11-digit product format
- 722050269
- Labeler code
- 72205
- Product ID
- 72205-269_11ca0e1d-1c0d-4357-9ebd-ee1e87185dde
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- brivaracetam
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Novadoz Pharmaceuticals LLC
- Application
- ANDA214921
- Marketing category
- ANDA
- Marketing start
- 2025-11-13
- Substance
- BRIVARACETAM
- Active strength
- 50 mg/1
- Pharmacologic classes
- Epoxide Hydrolase Inhibitors [MoA]
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- brivaracetam
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BRIVARACETAM | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U863JGG2IA |
| Rxcui | 1739761, 1739768, 1739772, 1739776, 1739780 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72205-269-06 | brivaracetam | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 1 |
| 72205-269-06 | brivaracetam | 100 in 1 CARTON | TABLET, FILM COATED | 100 | | 1 |
| 72205-269-60 | brivaracetam | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72205-269-06 | 72205026906 | 100 BLISTER PACK in 1 CARTON (72205-269-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK | 100 blister pack | 2026-02-01 | No | No | Current |
| 72205-269-60 | 72205026960 | 60 TABLET, FILM COATED in 1 BOTTLE (72205-269-60) | | 2026-02-01 | No | No | Current |