1. Home
  2. Labeler Index
  3. Jerome Stevens Pharmaceuticals, Inc.
  4. NDC Product Code: 50564-554 Orphenadrine Citrate Aspirin Caffeine

NDC 50564-554 Orphenadrine Citrate Aspirin Caffeine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50564-554?
  5. Orphenadrine Citrate Aspirin 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:
50564-554
Proprietary Name:
Orphenadrine Citrate Aspirin Caffeine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jerome Stevens Pharmaceuticals, Inc.
Labeler Code:
50564
Product Label ID:
b49dd596-1f6a-4ff7-8079-e55bbcca8fbd
Start Marketing Date: [9]
04-30-1999
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329 - GREEN)
WHITE (C48325 - WHITE)
YELLOW (C48330 - YELLOW)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
JSP;554
Score:
1

Code Structure Chart

Product Details

What is NDC 50564-554?

The NDC code 50564-554 is assigned by the FDA to the product Orphenadrine Citrate Aspirin Caffeine which is product labeled by Jerome Stevens Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 50564-554-01 100 tablet in 1 bottle , 50564-554-05 500 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 Orphenadrine Citrate Aspirin Caffeine?

Symptomatic relief of mild to moderate pain of acute musculoskeletal disorders. The orphenadrine component is indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute painful musculoskeletal conditions. The mode of action of orphenadrine has not been clearly identified, but may be related to its analgesic properties. These products do not directly relax tense skeletal muscles in man.

Which are Orphenadrine Citrate Aspirin Caffeine UNII Codes?

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

Which are Orphenadrine Citrate Aspirin 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 Orphenadrine Citrate Aspirin 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: 994528 - orphenadrine citrate 25 MG / aspirin 385 MG / caffeine 30 MG Oral Tablet
  • RxCUI: 994528 - aspirin 385 MG / caffeine 30 MG / orphenadrine citrate 25 MG Oral Tablet
  • RxCUI: 994528 - ASA 385 MG / Caffeine 30 MG / Orphenadrine Citrate 25 MG Oral Tablet
  • RxCUI: 994535 - orphenadrine citrate 50 MG / aspirin 770 MG / caffeine 60 MG Oral Tablet
  • RxCUI: 994535 - aspirin 770 MG / caffeine 60 MG / orphenadrine citrate 50 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".