Methylphenidate Hydrochloride
- Product NDC
- 72162-1993
- 11-digit product format
- 721621993
- Labeler code
- 72162
- Product ID
- 72162-1993_50665123-f626-446e-81fa-bfef2a96dd23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylphenidate Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210139
- Marketing category
- ANDA
- Marketing start
- 2019-03-29
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 10 mg/5mL
- 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 |
|---|
| 4B3SC438HI | METHYLPHENIDATE HYDROCHLORIDE | 23655-65-4 | METHYLPHENIDATE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1993-5 | 72162199305 | 500 mL in 1 BOTTLE (72162-1993-5) | 500 ml | 2024-02-05 | No | No | Historical |