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  2. Altura Pharmaceuticals, Inc.
  3. NDC Product Code: 63874-861 Hydrocodone Bitartrate And Acetaminophen

NDC 63874-861 Hydrocodone Bitartrate And Acetaminophen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. Product Characteristics
    4. What is NDC 63874-861?
    5. Hydrocodone Bitartrate And Acetaminophen 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:
63874-861
Proprietary Name:
Hydrocodone Bitartrate And Acetaminophen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Altura Pharmaceuticals, Inc.
Labeler Code:
63874
Product Label ID:
047af99e-1c90-4de3-9116-b29ac4cd85d3
Start Marketing Date: [9]
01-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
WHITE (C48325 - WITH GREEN SPECKS)
YELLOW (C48330 - LIGHT YELLOW)
PINK (C48328)
BLUE (C48333 - LIGHT BLUE)
Shape:
OVAL (C48345)
Size(s):
17 MM
14 MM
16 MM
Imprint(s):
3592;V
3594;V
3596;V
3601;V
3600;V
3597;V
Score:
2
1

Product Packages

NDC Code 63874-861-01

Package Description: 100 TABLET in 1 BOTTLE, PLASTIC

NDC Code 63874-861-30

Package Description: 30 TABLET in 1 BOTTLE, PLASTIC

NDC Code 63874-861-60

Package Description: 60 TABLET in 1 BOTTLE, PLASTIC

NDC Code 63874-861-90

Package Description: 90 TABLET in 1 BOTTLE, PLASTIC

Product Details

What is NDC 63874-861?

The NDC code 63874-861 is assigned by the FDA to the product Hydrocodone Bitartrate And Acetaminophen which is product labeled by Altura Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 63874-861-01 100 tablet in 1 bottle, plastic , 63874-861-30 30 tablet in 1 bottle, plastic , 63874-861-60 60 tablet in 1 bottle, plastic , 63874-861-90 90 tablet 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 Hydrocodone Bitartrate And Acetaminophen?

Hydrocodone bitartrate and acetaminophen tablets are indicated for the relief of moderate to moderately severe pain.

Which are Hydrocodone Bitartrate And Acetaminophen UNII Codes?

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

Which are Hydrocodone Bitartrate And Acetaminophen 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 Hydrocodone Bitartrate And Acetaminophen?

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: 833036 - HYDROcodone bitartrate 7.5 MG / acetaminophen 750 MG Oral Tablet
  • RxCUI: 833036 - acetaminophen 750 MG / hydrocodone bitartrate 7.5 MG Oral Tablet
  • RxCUI: 833036 - APAP 750 MG / hydrocodone bitartrate 7.5 MG Oral Tablet
  • RxCUI: 856903 - HYDROcodone bitartrate 5 MG / acetaminophen 500 MG Oral Tablet
  • RxCUI: 856903 - acetaminophen 500 MG / hydrocodone bitartrate 5 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".