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  4. NDC Product Code: 55056-1601 Prochieve

NDC 55056-1601 Prochieve

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 55056-1601?
  5. Prochieve 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:
55056-1601
Proprietary Name:
Prochieve
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Columbia Laboratories
Labeler Code:
55056
Product Label ID:
9f8dc923-65d7-42ff-b718-97e7a7e87822
Start Marketing Date: [9]
05-13-1997
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 55056-1601?

The NDC code 55056-1601 is assigned by the FDA to the product Prochieve which is product labeled by Columbia Laboratories. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 55056-1601-5 15 applicator in 1 carton / 1.125 g in 1 applicator, 55056-1601-6 6 applicator in 1 carton / 1.125 g in 1 applicator, 55056-1601-8 18 applicator in 1 carton / 1.125 g in 1 applicator. 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 Prochieve?

Prochieve® should not be used in individuals with any of the following conditions:Known sensitivity to Prochieve® (progesterone or any of the other ingredients)Undiagnosed vaginal bleedingLiver dysfunction or diseaseKnown or suspected malignancy of the breast or genital organsMissed abortionActive thrombophlebitis or thromboembolic disorders, or a history of hormone-associated thrombophlebitis or thromboembolic disorders

Which are Prochieve UNII Codes?

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

Which are Prochieve 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 Prochieve?

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:

* 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".