Methylphenidate Hydrochloride
- Product NDC
- 71335-0838
- 11-digit product format
- 713350838
- Labeler code
- 71335
- Product ID
- 71335-0838_d70af836-f906-4fca-9bd7-f965da8a2ea3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylphenidate hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA010187
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1955-12-31
- Marketing end
- 0000-00-00
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0838-1 | 71335083801 | 30 TABLET in 1 BOTTLE (71335-0838-1) | 30 tablet | 2010-02-26 | 0000-00-00 | No | No | Current |
| 71335-0838-2 | 71335083802 | 90 TABLET in 1 BOTTLE (71335-0838-2) | 90 tablet | 2010-02-26 | 0000-00-00 | No | No | Current |
| 71335-0838-3 | 71335083803 | 60 TABLET in 1 BOTTLE (71335-0838-3) | 60 tablet | 2010-02-26 | 0000-00-00 | No | No | Current |