Dexmethylphenidate Hydrochloride
- Product NDC
- 72162-1286
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dexmethylphenidate hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207901
- Marketing category
- ANDA
- Substance
- DEXMETHYLPHENIDATE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 72162-1286-1 | 100 TABLET in 1 BOTTLE, PLASTIC (72162-1286-1) | 2024-02-01 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Dexmethylphenidate Hydrochloride | Bryant Ranch Prepack | 2024-02-01 | HUMAN PRESCRIPTION DRUG LABEL | 100 |