Methylphenidate Hydrochloride
- Product NDC
- 72162-2040
- 11-digit product format
- 721622040
- Labeler code
- 72162
- Product ID
- 72162-2040_d2d71458-ab2e-4d49-b988-481f0764f9df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylphenidate Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091601
- Marketing category
- ANDA
- Marketing start
- 2015-03-04
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 5 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 |
|---|
| 72162-2040-5 | 72162204005 | 500 mL in 1 BOTTLE, PLASTIC (72162-2040-5) | 500 ml | 2024-04-03 | No | No | Historical |