Droxidopa
- Product NDC
- 0054-0532
- 11-digit product format
- 000540532
- Labeler code
- 0054
- Product ID
- 0054-0532_32e24bbf-d284-4365-9aab-947496046910
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Droxidopa
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA212835
- Marketing category
- ANDA
- Marketing start
- 2021-02-18
- Marketing end
- 0000-00-00
- Substance
- DROXIDOPA
- Active strength
- 100 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 |
|---|
| 0054-0532-22 | 00054053222 | 90 CAPSULE in 1 BOTTLE (0054-0532-22) | 90 capsule | 2021-02-18 | 0000-00-00 | No | No | Current |