DRONABINOL
- Product NDC
- 0904-6746
- 11-digit product format
- 009046746
- Labeler code
- 0904
- Product ID
- 0904-6746_5ed39c1a-efd8-4996-9cf1-273474f9553a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DRONABINOL
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA078292
- Marketing category
- ANDA
- Marketing start
- 2018-06-26
- Marketing end
- 2023-01-31
- 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 |
|---|
| 0904-6746-04 | 00904674604 | 30 BLISTER PACK in 1 CARTON (0904-6746-04) > 1 CAPSULE in 1 BLISTER PACK | 30 blister pack | 2018-06-26 | 2023-01-31 | No | No | Current |