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  4. NDC Product Code: 0178-0893 Citranatal Assure

NDC 0178-0893 Citranatal Assure

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0178-0893?
  5. Citranatal Assure 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:
0178-0893
Proprietary Name:
Citranatal Assure
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mission Pharmacal Company
Labeler Code:
0178
Product Label ID:
40480393-700d-4afd-8309-704ac8689e85
Start Marketing Date: [9]
11-19-2008
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
ORANGE (C48331 - CLEAR, AMBER TO LIGHT/DARK ORANGE)
Shape:
OVAL (C48345)
CAPSULE (C48336)
Size(s):
20 MM
23 MM
Imprint(s):
0893
Score:
1

Code Structure Chart

Product Details

What is NDC 0178-0893?

The NDC code 0178-0893 is assigned by the FDA to the product Citranatal Assure 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 0178-0893-30 6 blister pack in 1 carton / 1 kit in 1 blister pack. 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 Assure?

CitraNatal Assure® 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 Assure UNII Codes?

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

Which are Citranatal Assure 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 Citranatal Assure?

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: 1304490 - alpha-tocopherol acetate 30 UNT / ascorbic acid 120 MG / calcium citrate 125 MG / cholecalciferol 400 UNT / cupric oxide 2 MG / docusate sodium 50 MG / folic acid 1 MG / iron carbonyl 35 MG / niacinamide 20 MG / potassium iodide 0.15 MG / pyridoxine hydrochloride 25 MG / riboflavin 3.4 MG / thiamine hydrochloride 3 MG / zinc oxide 25 MG Oral Tablet
  • RxCUI: 1304490 - alpha-Tocopherol Acetate 30 UNT / vitamin C 120 MG / Calcium Citrate 125 MG / Cholecalciferol 400 UNT / Cupric oxide 2 MG / DOSS Sodium 50 MG / folate 1 MG / Iron Carbonyl 35 MG / Niacinamide 20 MG / K+ Iodide 0.15 MG / vitamin B6 Hydrochloride 25 MG / Riboflavin 3.4 MG / vitamin B1 hydrochloride 3 MG / ZNO 25 MG Oral Tablet
  • RxCUI: 1304490 - alpha-Tocopherol Acetate 30 UNT / vitamin C 120 MG / Calcium Citrate 125 MG / Cholecalciferol 400 UNT / Cupric oxide 2 MG / DOSS Sodium 50 MG / folate 1 MG / Iron Carbonyl 35 MG / Niacinamide 20 MG / K+ Iodide 0.15 MG / vitamin B6 Hydrochloride 25 MG / Riboflavin 3.4 MG / vit-B1 hydrochloride 3 MG / ZNO 25 MG Oral Tablet
  • RxCUI: 1304490 - alpha-Tocopherol Acetate 30 UNT / vitamin C 120 MG / Calcium Citrate 125 MG / Cholecalciferol 400 UNT / Cupric oxide 2 MG / DOSS Sodium 50 MG / folate 1 MG / Iron Carbonyl 35 MG / Niacinamide 20 MG / K+ Iodide 0.15 MG / vit-B6 Hydrochloride 25 MG / Riboflavin 3.4 MG / vitamin B1 hydrochloride 3 MG / ZNO 25 MG Oral Tablet
  • RxCUI: 1304490 - alpha-Tocopherol Acetate 30 UNT / vitamin C 120 MG / Calcium Citrate 125 MG / Cholecalciferol 400 UNT / Cupric oxide 2 MG / DOSS Sodium 50 MG / folate 1 MG / Iron Carbonyl 35 MG / Niacinamide 20 MG / K+ Iodide 0.15 MG / vit-B6 Hydrochloride 25 MG / Riboflavin 3.4 MG / vit-B1 hydrochloride 3 MG / ZNO 25 MG Oral Tablet

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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".