Marinol
- Product NDC
- 0051-0022
- 11-digit product format
- 000510022
- Labeler code
- 0051
- Product ID
- 0051-0022_b35d3e84-6f3c-f566-ee76-691936f050c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dronabinol
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- AbbVie Inc.
- Application
- NDA018651
- Marketing category
- NDA
- Marketing start
- 2010-07-13
- Marketing end
- 2021-01-31
- Substance
- DRONABINOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Cannabinoid [EPC],Cannabinoids [CS]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record