Dronabinol
- Product NDC
- 49884-869
- 11-digit product format
- 498840869
- Labeler code
- 49884
- Product ID
- 49884-869_8e792359-de7f-4875-9834-0d74bd6066ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dronabinol
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA078292
- Marketing category
- ANDA
- Marketing start
- 2008-06-27
- Marketing end
- 0000-00-00
- Substance
- DRONABINOL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cannabinoid [EPC],Cannabinoids [CS]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 49884-869-01 | 49884086901 | 100 CAPSULE in 1 BOTTLE (49884-869-01) | 100 capsule | 2008-06-27 | 0000-00-00 | No | No | Current |
| 49884-869-05 | 49884086905 | 500 CAPSULE in 1 BOTTLE (49884-869-05) | 500 capsule | 2008-06-27 | 0000-00-00 | No | No | Current |
| 49884-869-15 | 49884086915 | 25 CAPSULE in 1 BOTTLE (49884-869-15) | 25 capsule | 2008-06-27 | 0000-00-00 | No | No | Current |