Droxidopa
- Product NDC
- 0832-0720
- 11-digit product format
- 008320720
- Labeler code
- 0832
- Product ID
- 0832-0720_a4875e75-bce5-46d2-a6ce-dfac46d1baed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Droxidopa
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories, LLC
- Application
- ANDA213661
- 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
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0832-0720 | DROXIDOPA CAPSULE [UPSHER-SMITH LABORATORIES, LLC] | 2 | Legacy NDC | 20230526_b419da70-1b11-4fff-ba00-60234bd5d265.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0832-0720-90 | 00832072090 | 90 CAPSULE in 1 BOTTLE (0832-0720-90) | 90 capsule | 2021-02-18 | 0000-00-00 | No | No | Current |