LISDEXAMFETAMINE DIMESYLATE
- Product NDC
- 57664-046
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LISDEXAMFETAMINE DIMESYLATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA214484
- Marketing category
- ANDA
- Substance
- LISDEXAMFETAMINE DIMESYLATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 57664-046-88 | 100 CAPSULE in 1 BOTTLE (57664-046-88) | 2023-08-25 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LISDEXAMFETAMINE DIMESYLATE | Sun Pharmaceutical Industries, Inc. | Ohm Laboratories Inc. | 2023-12-01 | HUMAN PRESCRIPTION DRUG LABEL | 8 |