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  4. NDC Product Code: 0722-7029 Butalbital, Acetaminophen, And Caffeine

NDC 0722-7029 Butalbital, Acetaminophen, And Caffeine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0722-7029?
  5. Butalbital, Acetaminophen, And Caffeine Uses
  6. Active 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:
0722-7029
Proprietary Name:
Butalbital, Acetaminophen, And Caffeine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nexgen Pharma, Inc.
Labeler Code:
0722
Product Label ID:
611356c6-9cf6-4316-a9cb-e7756955755b
Start Marketing Date: [9]
11-16-2009
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329 - DARK GREEN CAP)
YELLOW (C48330 - YELLOW BODY)
Shape:
CAPSULE (C48336)
Size(s):
13 MM
Imprint(s):
AP;661
Score:
1

Code Structure Chart

Product Details

What is NDC 0722-7029?

The NDC code 0722-7029 is assigned by the FDA to the product Butalbital, Acetaminophen, And Caffeine which is product labeled by Nexgen Pharma, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 0722-7029-01 100 capsule in 1 bottle , 0722-7029-05 500 capsule 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 Butalbital, Acetaminophen, And Caffeine?

Butalbital, Acetaminophen and Caffeine capsules are indicated for the relief of the symptom complex of tension (or muscle contraction) headache.Evidence supporting the efficacy and safety of this combination product in the treatment of multiple recurrent headaches is unavailable. Caution in this regard is required because butalbital is habit-forming and potentially abusable.

Which are Butalbital, Acetaminophen, And Caffeine UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Butalbital, Acetaminophen, And Caffeine?

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: 889520 - butalbital 50 MG / acetaminophen 300 MG / caffeine 40 MG Oral Capsule
  • RxCUI: 889520 - acetaminophen 300 MG / butalbital 50 MG / caffeine 40 MG Oral Capsule
  • RxCUI: 889520 - APAP 300 MG / butalbital 50 MG / caffeine 40 MG Oral Capsule

* 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".