NDC 60219-1621 Metyrosine

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
60219-1621
Proprietary Name:
Metyrosine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amneal Pharmaceuticals Ny Llc
Labeler Code:
60219
Start Marketing Date: [9]
07-24-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333 - DARK BLUE OPAQUE CAP AND LIGHT BLUE OPAQUE BODY)
Shape:
CAPSULE (C48336)
Size(s):
21 MM
Imprint(s):
AA;05A
Score:
1

Product Packages

NDC Code 60219-1621-1

Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC

Product Details

What is NDC 60219-1621?

The NDC code 60219-1621 is assigned by the FDA to the product Metyrosine which is product labeled by Amneal Pharmaceuticals Ny Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60219-1621-1 100 capsule in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Metyrosine?

Metyrosine capsules are indicated in the treatment of patients with pheochromocytoma for:1.   Preoperative preparation of patients for surgery.2.   Management of patients when surgery is contraindicated.3.   Chronic treatment of patients with malignant pheochromocytoma.Metyrosine capsules are not recommended for the control of essential hypertension.

Which are Metyrosine UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Metyrosine?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[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".