Droxidopa
- Product NDC
- 69539-146
- 11-digit product format
- 695390146
- Labeler code
- 69539
- Product ID
- 69539-146_700c0bc6-b089-4478-8e62-4232cad2348e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Droxidopa
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- MSN LABORATORIES PRIVATE LIMITED
- Application
- ANDA211741
- Marketing category
- ANDA
- Marketing start
- 2021-02-19
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69539-146 | DROXIDOPA CAPSULE [MSN LABORATORIES PRIVATE LIMITED] | 1 | Legacy NDC | 20210222_700c0bc6-b089-4478-8e62-4232cad2348e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69539-146-05 | 69539014605 | 500 CAPSULE in 1 BOTTLE (69539-146-05) | 500 capsule | 2021-02-19 | 0000-00-00 | No | No | Current |
| 69539-146-90 | 69539014690 | 90 CAPSULE in 1 BOTTLE (69539-146-90) | 90 capsule | 2021-02-19 | 0000-00-00 | No | No | Current |