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  4. NDC Product Code: 66336-619 Butalbital, Aspirin And Caffeine

NDC 66336-619 Butalbital, Aspirin And Caffeine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 66336-619?
  5. Butalbital, Aspirin And Caffeine 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:
66336-619
Proprietary Name:
Butalbital, Aspirin And Caffeine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dispensing Solutions, Inc.
Labeler Code:
66336
Product Label ID:
657e4c4a-e50c-49f7-99b4-32395ec19bd8
Start Marketing Date: [9]
06-05-1979
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
WESTWARD;785
Score:
1

Product Packages

NDC Code 66336-619-30

Package Description: 30 TABLET in 1 BOTTLE, PLASTIC

NDC Code 66336-619-60

Package Description: 60 TABLET in 1 BOTTLE, PLASTIC

Product Details

What is NDC 66336-619?

The NDC code 66336-619 is assigned by the FDA to the product Butalbital, Aspirin And Caffeine which is product labeled by Dispensing Solutions, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 66336-619-30 30 tablet in 1 bottle, plastic , 66336-619-60 60 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 Butalbital, Aspirin And Caffeine?

Butalbital, aspirin, and caffeine tablets are indicated for the relief of the symptom complex of tension (or muscle contraction) headache.Evidence supporting the efficacy and safety of butalbital, aspirin, and caffeine 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, Aspirin And Caffeine UNII Codes?

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

Which are Butalbital, Aspirin And Caffeine 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 Butalbital, Aspirin 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: 238135 - butalbital 50 MG / aspirin 325 MG / caffeine 40 MG Oral Tablet
  • RxCUI: 238135 - aspirin 325 MG / butalbital 50 MG / caffeine 40 MG Oral Tablet
  • RxCUI: 238135 - ASA 325 MG / butalbital 50 MG / caffeine 40 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".