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 |