lisdexamfetamine dimesylate
- Product NDC
- 72162-2216
- 11-digit product format
- 721622216
- Labeler code
- 72162
- Product ID
- 72162-2216_a0de8320-488d-4cd2-b976-68067f7222fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lisdexamfetamine dimesylate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA214547
- Marketing category
- ANDA
- Marketing start
- 2023-08-25
- Substance
- LISDEXAMFETAMINE DIMESYLATE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| SJT761GEGS | LISDEXAMFETAMINE DIMESYLATE | 608137-33-3 | LISDEXAMFETAMINE DIMESYLATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2216-1 | 72162221601 | 100 CAPSULE in 1 BOTTLE (72162-2216-1) | 100 capsule | 2024-01-05 | No | No | Historical |