Methylphenidate Hydrochloride
- Product NDC
- 0781-5748
- 11-digit product format
- 007815748
- Labeler code
- 0781
- Product ID
- 0781-5748_af088d35-9328-467a-a290-b7e98061e50b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylphenidate hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- NDA010187
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1955-12-31
- Marketing end
- 2022-05-31
- Substance
- METHYLPHENIDATE 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
- 0000-00-00
- 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 |
|---|
| 0781-5748-01 | 00781574801 | 100 TABLET in 1 BOTTLE (0781-5748-01) | 100 tablet | 1955-12-31 | 2022-05-31 | No | No | Current |