Quillivant
- Product NDC
- 24478-210
- 11-digit product format
- 244780210
- Labeler code
- 24478
- Product ID
- 24478-210_3c243fb6-41ad-44b8-a644-1d5a9d3df322
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylphenidate hydrochloride
- Dosage form
- SUSPENSION, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NextWave Pharmaceuticals, Inc
- Application
- NDA202100
- Marketing category
- NDA
- Marketing start
- 2012-10-01
- Marketing end
- 0000-00-00
- Substance
- METHYLPHENIDATE HYDROCHLORIDE
- Active strength
- 900 mg/180mL
- Pharmacologic classes
- Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 24478-210-30 | 24478021030 | 1 BOTTLE in 1 CARTON (24478-210-30) > 180 mL in 1 BOTTLE | 1 bottle | 2012-10-01 | 0000-00-00 | No | No | Current |