Modafinil
- Product NDC
- 59115-069
- 11-digit product format
- 591150069
- Labeler code
- 59115
- Product ID
- 59115-069_820cdf60-3664-42fc-a17f-85f5b1894551
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- modafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hikma Pharmaceutical
- Application
- ANDA090543
- Marketing category
- ANDA
- Marketing start
- 2008-04-04
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record