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  4. NDC Product Code: 66213-542 Animi-3 With Vitamin D

NDC 66213-542 Animi-3 With Vitamin D

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 66213-542?
  5. Animi-3 With Vitamin D Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
66213-542
Proprietary Name:
Animi-3 With Vitamin D
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pbm Pharmaceuticals, Inc
Labeler Code:
66213
Product Label ID:
d77846ab-bce6-4646-8c09-ddfcf09898a3
Start Marketing Date: [9]
06-01-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
Shape:
OVAL (C48345)
Size(s):
20 MM
Imprint(s):
ANIMI;3D
Score:
1

Code Structure Chart

Product Details

What is NDC 66213-542?

The NDC code 66213-542 is assigned by the FDA to the product Animi-3 With Vitamin D which is product labeled by Pbm Pharmaceuticals, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66213-542-60 60 capsule in 1 bottle, plastic . 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 Animi-3 With Vitamin D?

This product is contraindicated in patients with a known hyper-sensitivity to any of the ingredients.

Which are Animi-3 With Vitamin D UNII Codes?

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

Which are Animi-3 With Vitamin D 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 Animi-3 With Vitamin D?

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: 1193037 - cholecalciferol 1000 UNT / folic acid 1 MG / omega-3 acid ethyl esters (USP) 500 MG / phytosterols 200 MG / pyridoxine hydrochloride 12.5 MG / vitamin B12 0.5 MG Oral Capsule
  • RxCUI: 1193037 - cholecalciferol 1000 UNT / folate 1 MG / omega-3 acid ethyl esters (USP) 500 MG / phytosterols 200 MG / vitamin B6 hydrochloride 12.5 MG / vitamin B12 0.5 MG Oral Capsule
  • RxCUI: 1193037 - cholecalciferol 1000 UNT / folate 1 MG / omega-3 acid ethyl esters (USP) 500 MG / phytosterols 200 MG / vit-B6 hydrochloride 12.5 MG / vitamin B12 0.5 MG Oral Capsule
  • RxCUI: 1193046 - cholecalciferol 1000 UNT / folic acid 1 MG / omega-3 acid ethyl esters (USP) 500 MG / phytosterols 200 MG / pyridoxine hydrochloride 12.5 MG / vitamin B12 0.5 MG Oral Capsule [Animi-3 with Vitamin D]
  • RxCUI: 1193046 - cholecalciferol 1000 UNT / folate 1 MG / omega-3 acid ethyl esters (USP) 500 MG / phytosterols 200 MG / vitamin B6 hydrochloride 12.5 MG / vitamin B12 0.5 MG Oral Capsule [Animi-3 with Vitamin D]

* Please review the disclaimer below.

Patient Education

Cholecalciferol (Vitamin D3)


Cholecalciferol (vitamin D3) is used as a dietary supplement when the amount of vitamin D in the diet is not enough. People most at risk for vitamin D deficiency are older adults, breastfed infants, people with dark skin, obese people, and those with limited sun exposure, or gastrointestinal disease (GI; affecting the stomach or intestines) such as Crohn's disease or celiac disease. Cholecalciferol (vitamin D3) is also used along with calcium to prevent and treat bone diseases such as rickets (softening and weakening of bones in children caused by lack of vitamin D), osteomalacia (softening and weakening of bones in adults caused by lack of vitamin D), and osteoporosis (a condition in which the bones become thin and weak and break easily). Cholecalciferol (vitamin D3) is in a class of medications called vitamin D analogs. Cholecalciferol is needed by the body for healthy bones, muscles, nerves, and to support the immune system. It works by helping the body to use more of the calcium found in foods or supplements.
[Learn More]


Omega-3 Fatty Acids


Omega-3 fatty acids are used together with lifestyle changes (diet, weight-loss, exercise) to reduce the amount of triglycerides (a fat-like substance) in the blood in people with very high triglycerides. Omega-3 fatty acids are in a class of medications called antilipemic or lipid-regulating agents. Omega-3 fatty acids may work by decreasing the amount of triglycerides and other fats made in the liver.
[Learn More]


Pyridoxine


Pyridoxine, vitamin B6, is required by your body for utilization of energy in the foods you eat, production of red blood cells, and proper functioning of nerves. It is used to treat and prevent vitamin B6 deficiency resulting from poor diet, certain medications, and some medical conditions. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]


* 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".