NDC 58607-112 Myferon 150 Forte
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 58607-112?
What are the uses for Myferon 150 Forte?
Which are Myferon 150 Forte UNII Codes?
The UNII codes for the active ingredients in this product are:
- IRON SUCROSE (UNII: FZ7NYF5N8L)
- FERRIC CATION (UNII: 91O4LML611) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
Which are Myferon 150 Forte 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- GELATIN (UNII: 2G86QN327L)
- CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SHELLAC (UNII: 46N107B71O)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Myferon 150 Forte?
- RxCUI: 309606 - polysaccharide iron complex (iron) 150 MG / folic acid 1 MG / vitamin B12 25 MCG Oral Capsule
- RxCUI: 309606 - folic acid 1 MG / polysaccharide iron complex 150 MG / vitamin B12 0.025 MG Oral Capsule
- RxCUI: 309606 - cyanocobalamin 25 MCG / folic acid 1 MG / polysaccharide iron complex 150 MG Oral Capsule
- RxCUI: 309606 - folate 1 MG / polysaccharide iron complex 150 MG / vitamin B12 0.025 MG Oral Capsule
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[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".