NDC 50090-3496 Amiodarone Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-3496 - Amiodarone Hydrochloride
Product Characteristics
Product Packages
NDC Code 50090-3496-1
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 50090-3496-2
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 50090-3496?
What are the uses for Amiodarone Hydrochloride?
Which are Amiodarone Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMIODARONE HYDROCHLORIDE (UNII: 976728SY6Z)
- AMIODARONE (UNII: N3RQ532IUT) (Active Moiety)
Which are Amiodarone Hydrochloride Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
What is the NDC to RxNorm Crosswalk for Amiodarone Hydrochloride?
- RxCUI: 833528 - amiodarone HCl 200 MG Oral Tablet
- RxCUI: 833528 - amiodarone hydrochloride 200 MG Oral Tablet
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Patient Education
Amiodarone
Amiodarone is used to treat and prevent certain types of serious, life-threatening ventricular arrhythmias (a certain type of abnormal heart rhythm when other medications did not help or could not be tolerated. Amiodarone is in a class of medications called antiarrhythmics. It works by relaxing overactive heart muscles.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".