ISOXSUPRINE HYDROCHLORIDE
- Product NDC
- 66576-201
- 11-digit product format
- 665760201
- Labeler code
- 66576
- Product ID
- 66576-201_78415673-7d9b-43dd-aedd-5e755ecf2151
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- isoxsuprine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Syntho Pharmaceuticals Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-06-11
- 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 |
|---|
| 66576-201-10 | 66576020110 | 100 TABLET in 1 BOTTLE (66576-201-10) | 100 tablet | 2020-06-11 | 0000-00-00 | No | No | Current |