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ISOXSUPRINE HYDROCHLORIDE
ISOXSUPRINE HYDROCHLORIDE - 61971-065-10 - (Isoxsuprine hydrochloride)
Drug Information of ISOXSUPRINE HYDROCHLORIDE
| Product NDC: | 61971-065 |
| Proprietary Name: | ISOXSUPRINE HYDROCHLORIDE |
| Non Proprietary Name: | Isoxsuprine hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; Isoxsuprine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ISOXSUPRINE HYDROCHLORIDE
| Product NDC: | 61971-065 |
| Labeler Name: | Vista Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19970919 |
Package Information of ISOXSUPRINE HYDROCHLORIDE
| Package NDC: | 61971-065-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (61971-065-10) |
NDC Information of ISOXSUPRINE HYDROCHLORIDE
| NDC Code | 61971-065-10 |
| Proprietary Name | ISOXSUPRINE HYDROCHLORIDE |
| Package Description | 1000 TABLET in 1 BOTTLE (61971-065-10) |
| Product NDC | 61971-065 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Isoxsuprine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19970919 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Vista Pharmaceuticals, Inc. |
| Substance Name | ISOXSUPRINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
