Modafinil
- Product NDC
- 71335-1793
- 11-digit product format
- 713351793
- Labeler code
- 71335
- Product ID
- 71335-1793_5b13a450-ca03-48bf-82fd-29f5374f7728
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Modafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078963
- Marketing category
- ANDA
- Marketing start
- 2013-08-01
- 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
- 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 |
|---|
| 71335-1793-1 | 71335179301 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-1793-1) | 30 tablet | 2021-03-10 | 0000-00-00 | No | No | Current |
| 71335-1793-2 | 71335179302 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-1793-2) | 60 tablet | 2021-03-10 | 0000-00-00 | No | No | Current |
| 71335-1793-3 | 71335179303 | 28 TABLET in 1 BOTTLE, PLASTIC (71335-1793-3) | 28 tablet | 2021-03-10 | 0000-00-00 | No | No | Current |
| 71335-1793-4 | 71335179304 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-1793-4) | 90 tablet | 2021-03-10 | 0000-00-00 | No | No | Current |
| 71335-1793-5 | 71335179305 | 45 TABLET in 1 BOTTLE, PLASTIC (71335-1793-5) | 45 tablet | 2022-02-14 | 0000-00-00 | No | No | Current |
| 71335-1793-6 | 71335179306 | 180 TABLET in 1 BOTTLE, PLASTIC (71335-1793-6) | 180 tablet | 2022-02-14 | 0000-00-00 | No | No | Current |