15455-9557 NDC - INFLA-EZE ()

Drug Information

  • Product NDC: 15455-9557
  • Proprietary Name: Infla-eze
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Alvix Laboratories, LLC
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:1/11/2016
End Marketing Date:1/28/2019

Package Information

No. Package Code Package Description Billing Unit
115455-9557-11 KIT in 1 CARTON (15455-9557-1) * 100 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC15455-9557Name of Company corresponding to the labeler code segment of the Product NDC.
PROPRIETARY NAMEInfla-ezeAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
START MARKETING DATE1/11/2016 
END MARKETING DATE1/28/2019 
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEAlvix Laboratories, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/21/2025

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