NDC 66336-408 Hydrocodone Bitartrate And Acetaminophen

Table of Contents

    1. Product Information
    2. Product Packages
    3. Product Characteristics
    4. What is NDC 66336-408?
    5. Hydrocodone Bitartrate And Acetaminophen Uses
    6. Active Ingredients UNII Codes
    7. Inactive Ingredients UNII Codes
    8. NDC to RxNorm Crosswalk

Product Information

NDC Product Code66336-408
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		Hydrocodone Bitartrate And Acetaminophen
NDC Directory StatusINACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Dispensing Solutions, Inc.
Labeler Code66336
SPL SET ID:0045ec13-789a-40a1-ac1f-8c29049cfd13
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		05-31-2000
Listing Expiration Date 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.		12-31-2017
Exclude Flag 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". 		I
NDC Code Structure

Product Characteristics

Color(s)PINK (C48328)
ShapeOVAL (C48345)
Size(s)17 MM
Imprint(s)3600;V
Score1

Product Packages

NDC Code 66336-408-15

Package Description: 15 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-408-20

Package Description: 20 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-408-28

Package Description: 28 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-408-30

Package Description: 30 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-408-32

Package Description: 32 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-408-40

Package Description: 40 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-408-55

Package Description: 150 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-408-60

Package Description: 60 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-408-62

Package Description: 180 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-408-90

Package Description: 90 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-408-94

Package Description: 120 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-408-97

Package Description: 150 TABLET in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

What is NDC 66336-408?

The NDC code 66336-408 is assigned by the FDA to the product Hydrocodone Bitartrate And Acetaminophen which is product labeled by Dispensing Solutions, Inc.. The product's dosage form is . The product is distributed in 12 packages with assigned NDC codes 66336-408-15 15 tablet in 1 bottle, plastic , 66336-408-20 20 tablet in 1 bottle, plastic , 66336-408-28 28 tablet in 1 bottle, plastic , 66336-408-30 30 tablet in 1 bottle, plastic , 66336-408-32 32 tablet in 1 bottle, plastic , 66336-408-40 40 tablet in 1 bottle, plastic , 66336-408-55 150 tablet in 1 bottle, plastic , 66336-408-60 60 tablet in 1 bottle, plastic , 66336-408-62 180 tablet in 1 bottle, plastic , 66336-408-90 90 tablet in 1 bottle, plastic , 66336-408-94 120 tablet in 1 bottle, plastic , 66336-408-97 150 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: 857107 - HYDROcodone bitartrate 10 MG / acetaminophen 500 MG Oral Tablet
  • RxCUI: 857107 - acetaminophen 500 MG / hydrocodone bitartrate 10 MG Oral Tablet
  • RxCUI: 857107 - APAP 500 MG / hydrocodone bitartrate 10 MG Oral Tablet

* Please review the disclaimer below.

Product Label

We have moved the product label and warning information to a dedicated page, please follow the link below:

View Product Label