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  4. NDC Product Code: 12634-179 Methergine

NDC 12634-179 Methergine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 12634-179?
  5. Methergine Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
12634-179
Proprietary Name:
Methergine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Apotheca, Inc.
Labeler Code:
12634
Product Label ID:
b91d1729-2e8e-4398-9a0d-02763bcfe284
Start Marketing Date: [9]
12-27-2006
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327 - ORCHID)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
78;54;SANDOZ
Score:
1

Product Packages

NDC Code 12634-179-00

Package Description: 10 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Code 12634-179-80

Package Description: 20 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Code 12634-179-82

Package Description: 12 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Code 12634-179-85

Package Description: 15 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Code 12634-179-91

Package Description: 1 TABLET, COATED in 1 BLISTER PACK

NDC Code 12634-179-96

Package Description: 6 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Code 12634-179-98

Package Description: 8 TABLET, COATED in 1 BOTTLE, PLASTIC

Product Details

What is NDC 12634-179?

The NDC code 12634-179 is assigned by the FDA to the product Methergine which is product labeled by Apotheca, Inc.. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 12634-179-00 10 tablet, coated in 1 bottle, plastic , 12634-179-80 20 tablet, coated in 1 bottle, plastic , 12634-179-82 12 tablet, coated in 1 bottle, plastic , 12634-179-85 15 tablet, coated in 1 bottle, plastic , 12634-179-91 1 tablet, coated in 1 blister pack , 12634-179-96 6 tablet, coated in 1 bottle, plastic , 12634-179-98 8 tablet, coated 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 Methergine?

This medication is used after childbirth to help stop bleeding from the uterus. Methylergonovine belongs to a class of drugs known as ergot alkaloids. It works by increasing the rate and strength of contractions and the stiffness of the uterus muscles. These effects help to decrease bleeding.

Which are Methergine UNII Codes?

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

Which are Methergine 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 Methergine?

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".