ISOXSUPRINE HYDROCHLORIDE
- Product NDC
- 51293-605
- 11-digit product format
- 512930605
- Labeler code
- 51293
- Product ID
- 51293-605_7b894aa8-9fb0-49c7-b411-1467cdc50777
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- isoxsuprine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ECI Pharmaceuticals LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-08-23
- Marketing end
- 2025-03-31
- Substance
- ISOXSUPRINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 51293-605-01 | 51293060501 | 100 TABLET in 1 BOTTLE (51293-605-01) | 100 tablet | 2011-08-23 | 2025-03-31 | No | No | Current |
| 51293-605-10 | 51293060510 | 1000 TABLET in 1 BOTTLE, PLASTIC (51293-605-10) | 1000 tablet | 2011-08-23 | 2025-03-31 | No | No | Current |