Droxidopa
- Product NDC
- 72606-019
- 11-digit product format
- 726060019
- Labeler code
- 72606
- Product ID
- 72606-019_0ce22c0b-5990-421f-9df4-ea3cfa022bff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Droxidopa
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- CELLTRION USA, INC.
- Application
- ANDA214217
- Marketing category
- ANDA
- Marketing start
- 2022-05-18
- Marketing end
- 0000-00-00
- Substance
- DROXIDOPA
- Active strength
- 200 mg/1
- Pharmacologic classes
- Catecholamines [CS], Increased Blood Pressure [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 72606-019-01 | 72606001901 | 90 CAPSULE in 1 BOTTLE (72606-019-01) | 90 capsule | 2022-05-18 | 0000-00-00 | No | No | Current |