Selenious Acid is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by American Regent, Inc.. The primary component is Selenium.
| Product ID | 0517-6560_03e692ec-1d5a-4944-af36-a25c04dd86c1 |
| NDC | 0517-6560 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Selenious Acid |
| Generic Name | Selenious Acid |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2019-07-01 |
| Marketing Category | NDA / NDA |
| Application Number | NDA209379 |
| Labeler Name | American Regent, Inc. |
| Substance Name | SELENIUM |
| Active Ingredient Strength | 60 ug/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2019-07-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA209379 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2019-07-01 |
| Marketing Category | NDA |
| Application Number | NDA209379 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2019-07-01 |
| Marketing End Date | 2019-11-06 |
| Marketing Category | NDA |
| Application Number | NDA209379 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2019-07-01 |
| Ingredient | Strength |
|---|---|
| SELENIUM | 60 ug/mL |
| SPL SET ID: | 49324999-50e3-43ed-a8dd-156d6dbedd9f |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0517-6502 | Selenious Acid | Selenious Acid |
| 0517-6560 | Selenious Acid | Selenious Acid |
| 69784-840 | Selenious Acid | Selenious Acid |