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  4. NDC Product Code: 0178-0812 Citranatal Harmony

NDC 0178-0812 Citranatal Harmony

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0178-0812?
  5. Citranatal Harmony Uses
  6. Active 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:
0178-0812
Proprietary Name:
Citranatal Harmony
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mission Pharmacal Company
Labeler Code:
0178
Product Label ID:
76ad10bd-3a53-4df5-b1c4-c98dbebe2fed
Start Marketing Date: [9]
04-27-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327 - OPAQUE)
Shape:
CAPSULE (C48336)
Size(s):
25 MM
Imprint(s):
812
Score:
1

Code Structure Chart

Product Details

What is NDC 0178-0812?

The NDC code 0178-0812 is assigned by the FDA to the product Citranatal Harmony which is product labeled by Mission Pharmacal Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0178-0812-30 1 bottle in 1 carton / 30 capsule, gelatin coated 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 Citranatal Harmony?

CitraNatal® Harmony™ is a multivitamin/mineral prescription drug indicated for use in improving the nutritional status of women prior to conception, throughout pregnancy, and in the postnatal period for both lactating and nonlactating mothers.

Which are Citranatal Harmony UNII Codes?

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

* 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".