Modafinil
- Product NDC
- 50090-2473
- 11-digit product format
- 500902473
- Labeler code
- 50090
- Product ID
- 50090-2473_d3a2d594-035e-44bd-9037-c2320b358705
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Modafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202566
- Marketing category
- ANDA
- Marketing start
- 2012-09-27
- Marketing end
- 0000-00-00
- Substance
- MODAFINIL
- Active strength
- 200 mg/1
- Pharmacologic classes
- Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 50090-2473-0 | 50090247300 | 30 TABLET in 1 BOTTLE (50090-2473-0) | 30 tablet | 2016-09-23 | 0000-00-00 | No | No | Current |