Rufinamide
- Product NDC
- 60687-643
- 11-digit product format
- 606870643
- Labeler code
- 60687
- Product ID
- 60687-643_e0c90c5c-48fe-5369-e053-2a95a90a9d0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rufinamide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA205075
- Marketing category
- ANDA
- Marketing start
- 2022-06-20
- Marketing end
- 0000-00-00
- Substance
- RUFINAMIDE
- Active strength
- 400 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-643-21 | 60687064321 | 30 BLISTER PACK in 1 CARTON (60687-643-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-643-11) | 30 blister pack | 2022-06-20 | 0000-00-00 | No | No | Current |