ISOXSUPRINE HYDROCHLORIDE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Syntho Pharmaceuticals Inc.. The primary component is Isoxsuprine Hydrochloride.
| Product ID | 66576-101_67123d7e-25c1-415c-bd8a-562fe3df76eb |
| NDC | 66576-101 |
| Product Type | Human Prescription Drug |
| Proprietary Name | ISOXSUPRINE HYDROCHLORIDE |
| Generic Name | Isoxsuprine Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2020-02-06 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Syntho Pharmaceuticals Inc. |
| Substance Name | ISOXSUPRINE HYDROCHLORIDE |
| Active Ingredient Strength | 10 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2020-02-06 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 42582-100 | ISOXSUPRINE HYDROCHLORIDE | isoxsuprine hydrochloride |
| 42582-101 | ISOXSUPRINE HYDROCHLORIDE | isoxsuprine hydrochloride |
| 42582-200 | ISOXSUPRINE HYDROCHLORIDE | isoxsuprine hydrochloride |
| 42582-201 | ISOXSUPRINE HYDROCHLORIDE | isoxsuprine hydrochloride |
| 51293-605 | ISOXSUPRINE HYDROCHLORIDE | isoxsuprine hydrochloride |
| 51293-606 | ISOXSUPRINE HYDROCHLORIDE | isoxsuprine hydrochloride |
| 61971-065 | ISOXSUPRINE HYDROCHLORIDE | Isoxsuprine hydrochloride |
| 63549-919 | ISOXSUPRINE HYDROCHLORIDE | isoxsuprine hydrochloride |
| 66576-101 | ISOXSUPRINE HYDROCHLORIDE | isoxsuprine hydrochloride |
| 66576-201 | ISOXSUPRINE HYDROCHLORIDE | isoxsuprine hydrochloride |