ISOXSUPRINE HYDROCHLORIDE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Vista Pharmaceuticals, Inc.. The primary component is Isoxsuprine Hydrochloride.
| Product ID | 61971-065_41a938f9-f98f-4208-a9a2-fd6097df087e |
| NDC | 61971-065 |
| Product Type | Human Prescription Drug |
| Proprietary Name | ISOXSUPRINE HYDROCHLORIDE |
| Generic Name | Isoxsuprine Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 1997-09-19 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Vista Pharmaceuticals, Inc. |
| Substance Name | ISOXSUPRINE HYDROCHLORIDE |
| Active Ingredient Strength | 20 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 1997-09-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-09-19 |
| Ingredient | Strength |
|---|---|
| ISOXSUPRINE HYDROCHLORIDE | 20 mg/1 |
| SPL SET ID: | e6582e24-9414-43b8-ac6f-b1422e3197cf |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| 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 |