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  4. NDC Product Code: 21695-690 Erythromycin Ethylsuccinate And Sulfisoxazole Acetyl

NDC 21695-690 Erythromycin Ethylsuccinate And Sulfisoxazole Acetyl

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 21695-690?
  5. Erythromycin Ethylsuccinate And Sulfisoxazole Acetyl 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:
21695-690
Proprietary Name:
Erythromycin Ethylsuccinate And Sulfisoxazole Acetyl
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rebel Distributors Corp
Labeler Code:
21695
Product Label ID:
60d1aea0-f106-4b20-8ef4-7a80e37f8a50
Start Marketing Date: [9]
05-20-1988
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375)

Code Structure Chart

Product Details

What is NDC 21695-690?

The NDC code 21695-690 is assigned by the FDA to the product Erythromycin Ethylsuccinate And Sulfisoxazole Acetyl which is product labeled by Rebel Distributors Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 21695-690-00 100 ml 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 Erythromycin Ethylsuccinate And Sulfisoxazole Acetyl?

For treatment of ACUTE OTITIS MEDIA in children that is caused by susceptible strains of Haemophilus influenzae.

Which are Erythromycin Ethylsuccinate And Sulfisoxazole Acetyl UNII Codes?

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

Which are Erythromycin Ethylsuccinate And Sulfisoxazole Acetyl 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 Erythromycin Ethylsuccinate And Sulfisoxazole Acetyl?

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: 686383 - erythromycin ethylsuccinate 200 MG / sulfiSOXAZOLE 600 MG in 5 mL Oral Suspension
  • RxCUI: 686383 - erythromycin ethylsuccinate 40 MG/ML / sulfisoxazole 120 MG/ML Oral Suspension
  • RxCUI: 686383 - EES 40 MG/ML / Sulfisoxazole 120 MG/ML Oral Suspension
  • RxCUI: 686383 - erythromycin ethylsuccinate 200 MG / sulfisoxazole 600 MG per 5 ML Oral Suspension

* 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".