Citranatal
NDC 0178-0866

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0178-0866?
  5. Citranatal B-calm 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.

Citranatal is a UNAPPROVED DRUG OTHER-approved product labeled by Mission Pharmacal Company. This medication is a multivitamin and iron product used to treat or prevent vitamin deficiency due to poor diet, certain illnesses, or during pregnancy. It is supplied as a white product. This product entry covers the primary NDC 0178-0866 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
0178-0866
Proprietary Name:
Citranatal B-calm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Mission Pharmacal Company
Labeler Code:
0178
Product Label ID:
b7846220-4137-4f1f-aea8-cd47e992a845
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.

Marketing Timeline

Start Marketing Date: [9]
02-10-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I

Product Characteristics

Color(s):
WHITE (C48325)
WHITE (C48325 - OFF-WHITE)
Shape:
OVAL (C48345)
ROUND (C48348)
Size(s):
19 MM
6 MM
Imprint(s):
0866
B;6
Score:
1

Code Structure Chart

Product Details

What is NDC 0178-0866?

The NDC code 0178-0866 is assigned by the FDA to the product Citranatal B-calm. This pharmaceutical product is labeled by Mission Pharmacal Company and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 0178-0866-30. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

This medication is a multivitamin and iron product used to treat or prevent vitamin deficiency due to poor diet, certain illnesses, or during pregnancy. Vitamins and iron are important building blocks of the body and help keep you in good health.

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 this product?

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: 1100262 - ascorbic acid 120 MG / calcium citrate 125 MG / cholecalciferol 400 UNT / folic acid 1 MG / iron carbonyl 20 MG / pyridoxine hydrochloride 25 MG Oral Tablet
  • RxCUI: 1100262 - calcium citrate 125 MG / folic acid 1 MG / iron carbonyl 20 MG / vitamin B6 25 MG / vitamin C 120 MG / vitamin D3 400 UNT Oral Tablet
  • RxCUI: 1100262 - vitamin C 120 MG / Calcium Citrate 125 MG / Cholecalciferol 400 UNT / folate 1 MG / Iron Carbonyl 20 MG / vitamin B6 Hydrochloride 25 MG Oral Tablet
  • RxCUI: 1100262 - vitamin C 120 MG / Calcium Citrate 125 MG / Cholecalciferol 400 UNT / folate 1 MG / Iron Carbonyl 20 MG / vit-B6 Hydrochloride 25 MG Oral Tablet
  • RxCUI: 1100262 - vit-C 120 MG / Calcium Citrate 125 MG / Cholecalciferol 400 UNT / folate 1 MG / Iron Carbonyl 20 MG / vitamin B6 Hydrochloride 25 MG Oral Tablet

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Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product 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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".