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 |