NDC 68210-1520 Ferrous Sulfate

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:
68210-1520
Proprietary Name:
Ferrous Sulfate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
68210
Start Marketing Date: [9]
12-15-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Shape:
TRIANGLE (C48353)
Size(s):
14 MM
Imprint(s):
FS
Score:
1

Code Structure Chart

Product Details

What is NDC 68210-1520?

The NDC code 68210-1520 is assigned by the FDA to the product Ferrous Sulfate which is product labeled by Spirit Pharmaceuticals,llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 68210-1520-0 1 bottle in 1 carton / 100 tablet, film coated in 1 bottle, 68210-1520-1 1 bag in 1 drum / 15000 tablet, film coated in 1 bag, 68210-1520-2 1 bag in 1 drum / 10000 tablet, film coated in 1 bag, 68210-1520-3 1 bag in 1 drum / 1000 tablet, film coated in 1 bag. 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 Ferrous Sulfate?

This medication is an iron supplement used to treat or prevent low blood levels of iron (such as those caused by anemia or pregnancy). Iron is an important mineral that the body needs to produce red blood cells and keep you in good health.

Which are Ferrous Sulfate UNII Codes?

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

Which are Ferrous Sulfate 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 Ferrous Sulfate?

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:

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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".