Dexmethylphenidate Hydrochloride
- Product NDC
- 72162-1285
- 11-digit product format
- 721621285
- Labeler code
- 72162
- Product ID
- 72162-1285_523810be-f07b-4274-b2e8-576c6124bee8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dexmethylphenidate hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207901
- Marketing category
- ANDA
- Marketing start
- 2001-11-30
- Substance
- DEXMETHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 5 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 |
|---|
| 1678OK0E08 | DEXMETHYLPHENIDATE HYDROCHLORIDE | 19262-68-1 | DEXMETHYLPHENIDATE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1285-1 | 72162128501 | 100 TABLET in 1 BOTTLE, PLASTIC (72162-1285-1) | 100 tablet | 2024-02-01 | No | No | Historical |