ISOXSUPRINE HYDROCHLORIDE
- Product NDC
- 66576-101
- 11-digit product format
- 665760101
- Labeler code
- 66576
- Product ID
- 66576-101_67123d7e-25c1-415c-bd8a-562fe3df76eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- isoxsuprine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Syntho Pharmaceuticals Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-02-06
- Marketing end
- 0000-00-00
- Substance
- ISOXSUPRINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 66576-101-10 | 66576010110 | 100 TABLET in 1 BOTTLE (66576-101-10) | 100 tablet | 2020-02-06 | 0000-00-00 | No | No | Current |