NDC 60219-1621 Metyrosine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60219 - Amneal Pharmaceuticals Ny Llc
- 60219-1621 - Metyrosine
Product Characteristics
Product Packages
NDC Code 60219-1621-1
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 60219-1621?
What are the uses for Metyrosine?
Which are Metyrosine UNII Codes?
The UNII codes for the active ingredients in this product are:
- METYROSINE (UNII: DOQ0J0TPF7)
- METYROSINE (UNII: DOQ0J0TPF7) (Active Moiety)
Which are Metyrosine 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:
- ALCOHOL (UNII: 3K9958V90M)
- AMMONIA (UNII: 5138Q19F1X)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GELATIN (UNII: 2G86QN327L)
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED (UNII: 2165RE0K14)
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Metyrosine?
- RxCUI: 197980 - metyroSINE 250 MG Oral Capsule
- RxCUI: 197980 - metyrosine 250 MG Oral Capsule
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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".