Felbamate
- Product NDC
- 72162-1771
- 11-digit product format
- 721621771
- Labeler code
- 72162
- Product ID
- 72162-1771_f9d33fef-2820-499d-b629-36a6ee87b650
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Felbamate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202284
- Marketing category
- ANDA
- Marketing start
- 2018-09-04
- Substance
- FELBAMATE
- Active strength
- 600 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Felbamate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FELBAMATE | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X72RBB02N8 |
| Rxcui | 198359 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1771-1 | Felbamate | 100 in 1 BOTTLE | TABLET | 100 | | 102 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1771 | FELBAMATE TABLET [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20241105_696e3cbb-a431-4f29-acbd-1db8e9aaef93.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1771-1 | 72162177101 | 100 TABLET in 1 BOTTLE (72162-1771-1) | 100 tablet | 2026-03-25 | No | No | Historical |