NDC 0517-6510

Selenium

Selenium

Selenium is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by American Regent, Inc.. The primary component is Selenious Acid.

• Product ID: 0517-6510_08d7aacf-6d5c-4873-87bc-25725c9ec7b9
• NDC: 0517-6510
• Product Type: Human Prescription Drug
• Proprietary Name: Selenium
• Generic Name: Selenium
• Dosage Form: Injection, Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 1990-09-30
• Marketing End Date: 2021-03-31
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: American Regent, Inc.
• Substance Name: SELENIOUS ACID
• Active Ingredient Strength: 65 ug/mL
• NDC Exclude Flag: N

Packaging

NDC 0517-6510-25

25 VIAL, SINGLE-DOSE in 1 TRAY (0517-6510-25) > 10 mL in 1 VIAL, SINGLE-DOSE

• Marketing Start Date: 1990-09-30
• Marketing End Date: 2021-03-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0517-6510-25 [00517651025]

Selenium INJECTION, SOLUTION

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 1990-09-30
• Marketing End Date: 2021-03-31

Drug Details

Active Ingredients

Ingredient	Strength
SELENIOUS ACID	65.4 ug/mL

OpenFDA Data

• SPL SET ID: db7454bc-4f18-4632-b771-2e86db889bae
• Manufacturer:
  • American Regent, Inc.
• UNII:
  • F6A27P4Q4R
• RxNorm Concept Unique ID - RxCUI:
  • 562352
• UPC Code:
  • 0305176510255

NDC Crossover Matching brand name "Selenium" or generic name "Selenium"

NDC	Brand Name	Generic Name
0517-6510	Selenium	Selenium
64117-182	Hoarse Cough	SELENIUM
0220-4622	Selenium metallicum	SELENIUM
0220-4628	Selenium metallicum	SELENIUM
0220-4631	Selenium metallicum	SELENIUM
0220-4632	Selenium metallicum	SELENIUM
0220-4639	Selenium metallicum	SELENIUM
0220-4640	Selenium metallicum	SELENIUM
68428-631	Selenium metallicum	SELENIUM
71919-620	Selenium metallicum	SELENIUM