NDC 67296-1555 Ferrous Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 67296-1555?
What are the uses for Ferrous Sulfate?
Which are Ferrous Sulfate UNII Codes?
The UNII codes for the active ingredients in this product are:
- FERROUS SULFATE (UNII: 39R4TAN1VT)
- FERROUS CATION (UNII: GW89581OWR) (Active Moiety)
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:
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- RIBOFLAVIN (UNII: TLM2976OFR)
- CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FOOD YELLOW 3 FREE ACID (UNII: G2B7JWK1GG)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE (UNII: 029TFK992N)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Ferrous Sulfate?
- RxCUI: 310325 - ferrous sulfate 325 MG (iron 65 MG) Oral Tablet
- RxCUI: 310325 - ferrous sulfate 325 MG Oral Tablet
- RxCUI: 310325 - ferrous sulfate 324 MG (iron 65 MG) Oral Tablet
- RxCUI: 310325 - FESO4 325 MG Oral Tablet
* Please review the disclaimer below.
[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".