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ISOXSUPRINE HYDROCHLORIDE
ISOXSUPRINE HYDROCHLORIDE - 51293-605-01 - (isoxsuprine hydrochloride)
Drug Information of ISOXSUPRINE HYDROCHLORIDE
| Product NDC: | 51293-605 |
| 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: | 51293-605 |
| Labeler Name: | ECI Pharmaceuticals LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110823 |
Package Information of ISOXSUPRINE HYDROCHLORIDE
| Package NDC: | 51293-605-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (51293-605-01) |
NDC Information of ISOXSUPRINE HYDROCHLORIDE
| NDC Code | 51293-605-01 |
| Proprietary Name | ISOXSUPRINE HYDROCHLORIDE |
| Package Description | 100 TABLET in 1 BOTTLE (51293-605-01) |
| Product NDC | 51293-605 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | isoxsuprine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110823 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | ECI Pharmaceuticals LLC |
| Substance Name | ISOXSUPRINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
