Evekeo ODT
- Product NDC
- 24338-045
- 11-digit product format
- 243380045
- Labeler code
- 24338
- Product ID
- 24338-045_be398468-6342-42d3-b9e8-41ff7c2f2514
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMPHETAMINE SULFATE
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Arbor Pharmaceuticals
- Application
- NDA209905
- Marketing category
- NDA
- Marketing start
- 2021-08-30
- Marketing end
- 0000-00-00
- Substance
- AMPHETAMINE SULFATE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- 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 |
|---|
| 24338-045-01 | 24338004501 | 1 CASE in 1 CARTON (24338-045-01) > 1 BLISTER PACK in 1 CASE (24338-045-30) > 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 1 case | 2021-08-30 | 0000-00-00 | No | No | Current |