METHYLPHENIDATE HYDROCHLORIDE
- Product NDC
- 16714-823
- 11-digit product format
- 167140823
- Labeler code
- 16714
- Product ID
- 16714-823_500c390c-83f0-4008-9a85-0bcca9480678
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHYLPHENIDATE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- 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
- 2022-12-31
- 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 |
|---|
| 16714-823-01 | 16714082301 | 100 TABLET in 1 BOTTLE (16714-823-01) | 100 tablet | 2015-10-01 | 0000-00-00 | No | No | Current |