Modafinil
- Product NDC
- 71335-0811
- 11-digit product format
- 713350811
- Labeler code
- 71335
- Product ID
- 71335-0811_72d3fe4c-3f03-4663-9ab6-3ec4c7222af7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- modafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090543
- Marketing category
- ANDA
- Marketing start
- 2012-09-26
- Marketing end
- 0000-00-00
- Substance
- MODAFINIL
- Active strength
- 100 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 |
|---|
| 71335-0811-1 | 71335081101 | 30 TABLET in 1 BOTTLE (71335-0811-1) | 30 tablet | 2018-05-08 | 0000-00-00 | No | No | Current |
| 71335-0811-2 | 71335081102 | 60 TABLET in 1 BOTTLE (71335-0811-2) | 60 tablet | 2018-05-08 | 0000-00-00 | No | No | Current |
| 71335-0811-3 | 71335081103 | 28 TABLET in 1 BOTTLE (71335-0811-3) | 28 tablet | 2018-05-08 | 0000-00-00 | No | No | Current |
| 71335-0811-4 | 71335081104 | 90 TABLET in 1 BOTTLE (71335-0811-4) | 90 tablet | 2018-05-08 | 0000-00-00 | No | No | Current |