ISOXSUPRINE HYDROCHLORIDE
- Product NDC
- 61971-065
- 11-digit product format
- 619710065
- Labeler code
- 61971
- Product ID
- 61971-065_c09c46c6-eeba-44f4-af74-383263210f6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Isoxsuprine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Vista Pharmaceuticals, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1997-09-19
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61971-065-10 | 61971006510 | 1000 TABLET in 1 BOTTLE (61971-065-10) | 1000 tablet | 1997-09-19 | 0000-00-00 | No | No | Current |