1. Home
  2. Labeler Index
  3. Keltman Pharmaceuticals Inc.
  4. NDC Product Code: 68387-236 Norco

NDC 68387-236 Norco

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68387-236?
  5. Norco 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:
68387-236
Proprietary Name:
Norco
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Keltman Pharmaceuticals Inc.
Labeler Code:
68387
Product Label ID:
566bd196-3c0c-4f05-9e2e-4803ad3126d4
Start Marketing Date: [9]
02-01-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WITH ORANGE SPECKS)
Shape:
CAPSULE (C48336)
Size(s):
17 MM
Imprint(s):
WATSON;3202
Score:
2

Code Structure Chart

Product Details

What is NDC 68387-236?

The NDC code 68387-236 is assigned by the FDA to the product Norco which is product labeled by Keltman Pharmaceuticals Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 68387-236-30 30 tablet in 1 bottle , 68387-236-90 90 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.

What are the uses for Norco?

This combination medication is used to relieve moderate to severe pain. It contains an opioid pain reliever (hydrocodone) and a non-opioid pain reliever (acetaminophen). Hydrocodone works in the brain to change how your body feels and responds to pain. Acetaminophen can also reduce a fever.

Which are Norco UNII Codes?

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

Which are Norco 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 Norco?

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: 857002 - HYDROcodone bitartrate 5 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 857002 - acetaminophen 325 MG / hydrocodone bitartrate 5 MG Oral Tablet
  • RxCUI: 857002 - APAP 325 MG / hydrocodone bitartrate 5 MG Oral Tablet
  • RxCUI: 857004 - NORCO 5 MG / 325 MG Oral Tablet
  • RxCUI: 857004 - acetaminophen 325 MG / hydrocodone bitartrate 5 MG Oral Tablet [Norco]

* 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".