Evekeo ODT
- Product NDC
- 24338-037
- 11-digit product format
- 243380037
- Labeler code
- 24338
- Product ID
- 24338-037_84fe08cc-dddd-4ab6-9d7a-f62076b924e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMPHETAMINE SULFATE
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Azurity Pharmaceuticals, Inc.
- Application
- NDA209905
- Marketing category
- NDA
- Marketing start
- 2019-06-28
- Marketing end
- 0000-00-00
- Substance
- AMPHETAMINE SULFATE
- Active strength
- 20 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 |
|---|
| 24338-037-02 | 24338003702 | 2 CASE in 1 CARTON (24338-037-02) > 1 BLISTER PACK in 1 CASE (24338-037-15) > 15 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 2 case | 2019-06-28 | 0000-00-00 | No | No | Current |