ISOXSUPRINE HYDROCHLORIDE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bi-coastal Pharma International Limited Liability Company. The primary component is Isoxsuprine Hydrochloride.
Product ID | 42582-101_881994e0-3c9f-4a80-849d-ad3f46f59ca8 |
NDC | 42582-101 |
Product Type | Human Prescription Drug |
Proprietary Name | ISOXSUPRINE HYDROCHLORIDE |
Generic Name | Isoxsuprine Hydrochloride |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2011-06-02 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | BI-COASTAL PHARMA INTERNATIONAL LIMITED LIABILITY COMPANY |
Substance Name | ISOXSUPRINE HYDROCHLORIDE |
Active Ingredient Strength | 10 mg/1 |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2011-06-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | Unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-06-02 |
Inactivation Date | 2020-01-31 |
Reactivation Date | 2020-03-03 |
Ingredient | Strength |
---|---|
ISOXSUPRINE HYDROCHLORIDE | 10 mg/1 |
SPL SET ID: | 18d6b14d-3ceb-4922-8d54-8c5b0fe23d7c |
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 |