Methylphenidate Hydrochloride
- Product NDC
- 71335-0892
- 11-digit product format
- 713350892
- Labeler code
- 71335
- Product ID
- 71335-0892_ce0e1a65-04c0-44f4-a335-77ced8d9f05b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylphenidate Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040300
- Marketing category
- ANDA
- Marketing start
- 1998-11-27
- Marketing end
- 0000-00-00
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 20 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0892-1 | 71335089201 | 30 TABLET in 1 BOTTLE (71335-0892-1) | 30 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0892-2 | 71335089202 | 100 TABLET in 1 BOTTLE (71335-0892-2) | 100 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0892-3 | 71335089203 | 90 TABLET in 1 BOTTLE (71335-0892-3) | 90 tablet | 2018-07-03 | 0000-00-00 | No | No | Current |
| 71335-0892-4 | 71335089204 | 60 TABLET in 1 BOTTLE (71335-0892-4) | 60 tablet | 2018-07-03 | 0000-00-00 | No | No | Current |
| 71335-0892-5 | 71335089205 | 120 TABLET in 1 BOTTLE (71335-0892-5) | 120 tablet | 2021-12-27 | 0000-00-00 | No | No | Current |