NDC 15631-0013 Aletris Farinosa

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
Proprietary Name:
Aletris Farinosa
Product Type: [3]
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
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Product Details

What is NDC 15631-0013?

The NDC code 15631-0013 is assigned by the FDA to the product Aletris Farinosa which is product labeled by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 15631-0013-0 100 pellet in 1 package , 15631-0013-1 200 pellet in 1 package , 15631-0013-2 400 pellet in 1 package , 15631-0013-3 750 pellet in 1 package , 15631-0013-4 2500 pellet in 1 package , 15631-0013-5 12500 pellet in 1 package . 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 Aletris Farinosa?

Condition listed above or as directed by the physician

Which are Aletris Farinosa UNII Codes?

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

Which are Aletris Farinosa 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:

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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".