ISOXSUPRINE HYDROCHLORIDE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Vedco Dba Valdar. The primary component is Isoxsuprine Hydrochloride.
| Product ID | 63549-919_e6f0f0dd-940a-490f-a404-56dd561264e6 |
| NDC | 63549-919 |
| Product Type | Human Prescription Drug |
| Proprietary Name | ISOXSUPRINE HYDROCHLORIDE |
| Generic Name | Isoxsuprine Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2011-08-23 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Vedco dba Valdar |
| Substance Name | ISOXSUPRINE HYDROCHLORIDE |
| Active Ingredient Strength | 20 mg/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2011-08-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-08-23 |
| Inactivation Date | 2019-11-13 |
| Ingredient | Strength |
|---|---|
| ISOXSUPRINE HYDROCHLORIDE | 20 mg/1 |
| SPL SET ID: | 908691b4-7950-4f3e-bbea-ea568fee7ac3 |
| 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 |