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  4. NDC Product Code: 27241-092 Rivastigmine Tartrate

NDC 27241-092 Rivastigmine Tartrate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 27241-092?
  5. Rivastigmine Tartrate 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:
27241-092
Proprietary Name:
Rivastigmine Tartrate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ajanta Pharma Limited
Labeler Code:
27241
Product Label ID:
3d257f22-b504-4707-9b29-5ce9032667ca
Start Marketing Date: [9]
09-28-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
ORANGE (C48331)
RED (C48326)
Shape:
CAPSULE (C48336)
Size(s):
18 MM
Imprint(s):
AP;RIV1;5
AP;RIV3;0
AP;RIV4;5
Score:
1

Code Structure Chart

Product Details

What is NDC 27241-092?

The NDC code 27241-092 is assigned by the FDA to the product Rivastigmine Tartrate which is product labeled by Ajanta Pharma Limited. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 27241-092-06 60 capsule in 1 bottle , 27241-092-50 500 capsule in 1 bottle . 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 Rivastigmine Tartrate?

Rivastigmine tartrate is contraindicated in patients with: known hypersensitivity to rivastigmine, other carbamate derivatives or other components of the formulation [see Description (11)]. a previous history of application site reaction with rivastigmine transdermal patch suggestive of allergic contact dermatitis, in the absence of negative allergy testing [see Warnings and Precautions (5.2)]. Isolated cases of generalized skin reactions have been described in postmarketing experience [see Adverse Reactions (6.2)].

Which are Rivastigmine Tartrate UNII Codes?

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

Which are Rivastigmine Tartrate 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 Rivastigmine Tartrate?

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".