Dronabinol
- Product NDC
- 0904-7068
- 11-digit product format
- 009047068
- Labeler code
- 0904
- Product ID
- 0904-7068_3d9fb1c2-93b2-4e0e-941c-f4a670fbd8aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dronabinol
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- NDA018651
- Marketing category
- NDA
- Marketing start
- 2017-05-10
- Marketing end
- 0000-00-00
- Substance
- DRONABINOL
- Active strength
- 3 mg/1
- Pharmacologic classes
- Cannabinoid [EPC],Cannabinoids [CS]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 0904-7068-61 | 00904706861 | 100 BLISTER PACK in 1 CARTON (0904-7068-61) > 1 CAPSULE in 1 BLISTER PACK | 100 blister pack | 2017-05-10 | 0000-00-00 | No | No | Current |