DRONABINOL
- Product NDC
- 42291-449
- 11-digit product format
- 422910449
- Labeler code
- 42291
- Product ID
- 42291-449_77794c6c-82e4-43d1-8126-b0776d80fa17
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dronabinol
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA207421
- Marketing category
- ANDA
- Marketing start
- 2020-03-16
- 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
- 2021-12-31
- 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 |
|---|
| 42291-449-60 | 42291044960 | 60 CAPSULE in 1 BOTTLE (42291-449-60) | 60 capsule | 2020-03-16 | 0000-00-00 | No | No | Current |