NDC 16590-022 Acetaminophen, Butalbital And Caffeine

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
16590-022
Proprietary Name:
Acetaminophen, Butalbital And Caffeine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Stat Rx Usa Llc
Labeler Code:
16590
Start Marketing Date: [9]
02-16-1988
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
WESTWARD;787
Score:
2

Product Packages

NDC Code 16590-022-15

Package Description: 15 TABLET in 1 BOTTLE, PLASTIC

NDC Code 16590-022-20

Package Description: 20 TABLET in 1 BOTTLE, PLASTIC

NDC Code 16590-022-30

Package Description: 30 TABLET in 1 BOTTLE, PLASTIC

NDC Code 16590-022-60

Package Description: 60 TABLET in 1 BOTTLE, PLASTIC

NDC Code 16590-022-72

Package Description: 120 TABLET in 1 BOTTLE, PLASTIC

NDC Code 16590-022-90

Package Description: 90 TABLET in 1 BOTTLE, PLASTIC

NDC Code 16590-022-99

Package Description: 500 TABLET in 1 BOTTLE, PLASTIC

Product Details

What is NDC 16590-022?

The NDC code 16590-022 is assigned by the FDA to the product Acetaminophen, Butalbital And Caffeine which is product labeled by Stat Rx Usa Llc. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 16590-022-15 15 tablet in 1 bottle, plastic , 16590-022-20 20 tablet in 1 bottle, plastic , 16590-022-30 30 tablet in 1 bottle, plastic , 16590-022-60 60 tablet in 1 bottle, plastic , 16590-022-72 120 tablet in 1 bottle, plastic , 16590-022-90 90 tablet in 1 bottle, plastic , 16590-022-99 500 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 Acetaminophen, Butalbital And Caffeine?

Butalbital, acetaminophen 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 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 Acetaminophen, Butalbital And Caffeine UNII Codes?

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

Which are Acetaminophen, Butalbital 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 Acetaminophen, Butalbital 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: 238154 - butalbital 50 MG / acetaminophen 325 MG / caffeine 40 MG Oral Tablet
  • RxCUI: 238154 - acetaminophen 325 MG / butalbital 50 MG / caffeine 40 MG Oral Tablet
  • RxCUI: 238154 - APAP 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".