methylphenidate Hydrochloride
- Product NDC
- 10147-0686
- 11-digit product format
- 101470686
- Labeler code
- 10147
- Product ID
- 10147-0686_5e2dbcde-b6a2-11ec-9a3d-d90cfed203d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylphenidate hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Patriot Pharmaceuticals, LLC.
- Application
- NDA021121
- Marketing category
- NDA
- Marketing start
- 2000-08-01
- Marketing end
- 0000-00-00
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 36 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10147-0686 | METHYLPHENIDATE HYDROCHLORIDE TABLET [PATRIOT PHARMACEUTICALS, LLC.] | 10 | Legacy NDC | 20231130_dad446b7-b26c-44f2-9e30-4cbd10d8b23c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10147-0686-1 | 10147068601 | 100 TABLET in 1 BOTTLE (10147-0686-1) | 100 tablet | 2019-02-18 | 0000-00-00 | No | No | Current |