Modafinil
- Product NDC
- 0904-6423
- 11-digit product format
- 009046423
- Labeler code
- 0904
- Product ID
- 0904-6423_ba79644c-c89d-41e9-9851-6dbde712564a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Modafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA076715
- Marketing category
- ANDA
- Marketing start
- 2013-04-03
- 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
- 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 |
|---|
| 0904-6423-04 | 00904642304 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-6423-04) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2013-04-03 | 0000-00-00 | No | No | Current |