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  4. NDC Product Code: 70261-517 Tim-lat -pf

NDC 70261-517 Tim-lat -pf

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70261-517?
  4. Active Ingredients UNII Codes
  5. Inactive Ingredients UNII Codes
  6. 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:
70261-517
Proprietary Name:
Tim-lat -pf
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Imprimisrx Nj
Labeler Code:
70261
Product Label ID:
6bb5e498-b27c-191a-e053-2a91aa0acab3
Start Marketing Date: [9]
01-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70261-517-05

Package Description: 5 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 70261-517?

The NDC code 70261-517 is assigned by the FDA to the product Tim-lat -pf which is product labeled by Imprimisrx Nj. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70261-517-05 5 ml in 1 bottle, dropper . 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 Tim-lat -pf UNII Codes?

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

Which are Tim-lat -pf 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:

  • SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)

What is the NDC to RxNorm Crosswalk for Tim-lat -pf?

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: 388054 - latanoprost 0.005 % / timolol 0.5 % Ophthalmic Solution
  • RxCUI: 388054 - latanoprost 0.05 MG/ML / timolol 5 MG/ML Ophthalmic Solution
  • RxCUI: 388054 - latanoprost 0.05 MG/ML / timolol (as timolol maleate) 5 MG/ML Ophthalmic Solution

* 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".