Dronabinol
- Product NDC
- 67877-569
- 11-digit product format
- 678770569
- Labeler code
- 67877
- Product ID
- 67877-569_39f1187e-9d4a-d7dc-da32-89162596cde5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dronabinol
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Ascend Laboratories, LLC
- Application
- NDA018651
- Marketing category
- NDA
- Marketing start
- 2017-05-10
- Marketing end
- 2021-04-30
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67877-569-60 | 67877056960 | 1 BOTTLE in 1 CARTON (67877-569-60) > 60 CAPSULE in 1 BOTTLE | 1 bottle | 2017-05-10 | 2021-04-30 | No | No | Current |