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  4. NDC Product Code: 57297-286 Abacavir Sulfate, Lamivudine And Zidovudine

NDC 57297-286 Abacavir Sulfate, Lamivudine And Zidovudine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 57297-286?
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
57297-286
Proprietary Name:
Abacavir Sulfate, Lamivudine And Zidovudine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lupin Limited
Labeler Code:
57297
Product Label ID:
18dc6cc7-ec64-4730-941c-8a9ad5dcb252
Start Marketing Date: [9]
12-17-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333 - BLUE-GREEN)
Shape:
OVAL (C48345)
Size(s):
22 MM
Imprint(s):
LU;N51
Score:
1

Code Structure Chart

Product Details

What is NDC 57297-286?

The NDC code 57297-286 is assigned by the FDA to the product Abacavir Sulfate, Lamivudine And Zidovudine which is product labeled by Lupin Limited. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 57297-286-01 1 bottle in 1 carton / 100 tablet in 1 bottle, 57297-286-02 1 bottle in 1 carton / 500 tablet in 1 bottle, 57297-286-07 1 bottle in 1 carton / 60 tablet 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.

Which are Abacavir Sulfate, Lamivudine And Zidovudine UNII Codes?

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

Which are Abacavir Sulfate, Lamivudine And Zidovudine 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 Abacavir Sulfate, Lamivudine And Zidovudine?

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:
  • RxCUI: 307650 - abacavir sulfate 300 MG / lamiVUDine 150 MG / zidovudine 300 MG Oral Tablet
  • RxCUI: 307650 - abacavir 300 MG / lamivudine 150 MG / zidovudine 300 MG Oral Tablet
  • RxCUI: 307650 - abacavir (as abacavir sulfate) 300 MG / 3TC 150 MG / AZT 300 MG Oral Tablet
  • RxCUI: 307650 - abacavir 300 MG / 3TC 150 MG / AZT 300 MG Oral Tablet

* Please review the disclaimer below.

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".