droxidopa
- Product NDC
- 27808-201
- 11-digit product format
- 278080201
- Labeler code
- 27808
- Product ID
- 27808-201_1fd63f37-1b0b-4d1f-945e-0eed2f891504
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- droxidopa
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Tris Pharma Inc
- Application
- ANDA214543
- Marketing category
- ANDA
- Marketing start
- 2021-05-05
- Marketing end
- 0000-00-00
- Substance
- DROXIDOPA
- Active strength
- 300 mg/1
- Pharmacologic classes
- Catecholamines [CS],Increased Blood Pressure [PE]
- 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 |
|---|
| 27808-201-01 | 27808020101 | 90 CAPSULE in 1 BOTTLE (27808-201-01) | 90 capsule | 2021-10-15 | 0000-00-00 | No | No | Current |
| 27808-201-19 | 27808020119 | 90 CAPSULE in 1 BOTTLE (27808-201-19) | 90 capsule | 2021-10-15 | 0000-00-00 | No | No | Current |