Dronabinol
- Product NDC
- 0904-6597
- 11-digit product format
- 009046597
- Labeler code
- 0904
- Product ID
- 0904-6597_2a48cd37-b7fe-46b2-bffd-63cbec2fd959
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dronabinol
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA078292
- Marketing category
- ANDA
- Marketing start
- 2008-06-27
- Marketing end
- 2020-01-31
- Substance
- DRONABINOL
- Active strength
- 3 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