ISOXSUPRINE HYDROCHLORIDE
- Product NDC
- 42582-201
- 11-digit product format
- 425820201
- Labeler code
- 42582
- Product ID
- 42582-201_a2344d62-64b9-4bd6-8f88-eef4e32897be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- isoxsuprine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BI-COASTAL PHARMA INTERNATIONAL LIMITED LIABILITY COMPANY
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-06-02
- Marketing end
- 0000-00-00
- Substance
- ISOXSUPRINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42582-201-10 | 42582020110 | 100 TABLET in 1 BOTTLE (42582-201-10) | 100 tablet | 2011-06-02 | 0000-00-00 | No | No | Current |
| 42582-201-20 | 42582020120 | 1000 TABLET in 1 BOTTLE (42582-201-20) | 1000 tablet | 2011-06-02 | 0000-00-00 | No | No | Current |