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  4. NDC Product Code: 50845-0169 Problen Estrogen And Progesterone

NDC 50845-0169 Problen Estrogen And Progesterone

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50845-0169?
  4. Problen Estrogen And Progesterone Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50845-0169
Proprietary Name:
Problen Estrogen And Progesterone
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Liddell Laboratories, Inc.
Labeler Code:
50845
Product Label ID:
02eff84a-7cf2-401d-914e-d84003f56760
Start Marketing Date: [9]
01-31-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50845-0169-3

Package Description: 1 CARTON in 1 CARTON / 1 BOTTLE, SPRAY in 1 CARTON (50845-0169-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0169-1)

Product Details

What is NDC 50845-0169?

The NDC code 50845-0169 is assigned by the FDA to the product Problen Estrogen And Progesterone which is product labeled by Liddell Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50845-0169-3 1 carton in 1 carton / 1 bottle, spray in 1 carton (50845-0169-2) / 30 ml in 1 bottle, spray (50845-0169-1). 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 Problen Estrogen And Progesterone?

INDICATIONS:  Temporarily supports the body to rebalance estrogen output.  Symptoms may include: mood swings, hot flashes, irritability, lack of energy.

Which are Problen Estrogen And Progesterone UNII Codes?

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

Which are Problen Estrogen And Progesterone 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:

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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".