METHYLPHENIDATE HYDROCHLORIDE
- Product NDC
- 63629-1922
- 11-digit product format
- 636291922
- Labeler code
- 63629
- Product ID
- 63629-1922_c0c27d32-75a5-47c1-84a0-7fcc1d961f5d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHYLPHENIDATE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207416
- Marketing category
- ANDA
- Marketing start
- 2015-10-01
- 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 |
|---|
| 63629-1922-1 | 63629192201 | 100 TABLET in 1 BOTTLE (63629-1922-1) | 100 tablet | 2021-01-14 | 0000-00-00 | No | No | Current |