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  4. NDC Product Code: 67781-251 Uniphyl

NDC 67781-251 Uniphyl

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67781-251?
  5. Uniphyl 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:
67781-251
Proprietary Name:
Uniphyl
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Purdue Pharmaceutical Products Lp
Labeler Code:
67781
Product Label ID:
c4c80b87-fc6e-436d-84de-7a0cd9d895eb
Start Marketing Date: [9]
09-01-1982
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
PF;U;400
Score:
2

Code Structure Chart

Product Details

What is NDC 67781-251?

The NDC code 67781-251 is assigned by the FDA to the product Uniphyl which is product labeled by Purdue Pharmaceutical Products Lp. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 67781-251-01 100 tablet in 1 bottle , 67781-251-05 500 tablet 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 Uniphyl?

Theophylline is indicated for the treatment of the symptoms and reversible airflow obstruction associated with chronic asthma and other chronic lung diseases, e.g., emphysema and chronic bronchitis.

Which are Uniphyl UNII Codes?

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

  • THEOPHYLLINE ANHYDROUS (UNII: 0I55128JYK)
  • THEOPHYLLINE ANHYDROUS (UNII: 0I55128JYK) (Active Moiety)

Which are Uniphyl 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 Uniphyl?

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: 313291 - theophylline 400 MG Extended Release Oral Tablet
  • RxCUI: 348472 - theophylline 600 MG Extended Release Oral Tablet
  • RxCUI: 844831 - Uniphyl Tablets 400 MG Extended Release Oral Tablet
  • RxCUI: 844831 - theophylline 400 MG Extended Release Oral Tablet [Uniphyl]
  • RxCUI: 844831 - Uniphyl 400 MG Extended Release 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".