NDC 0178-0716 Natafort
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0178 - Mission Pharmacal Company
- 0178-0716 - Natafort
Product Characteristics
Product Packages
NDC Code 0178-0716-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 0178-0716?
What are the uses for Natafort?
Which are Natafort UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) (Active Moiety)
- THIAMINE MONONITRATE (UNII: 8K0I04919X)
- THIAMINE (UNII: X66NSO3N35) (Active Moiety)
- RIBOFLAVIN (UNII: TLM2976OFR)
- RIBOFLAVIN (UNII: TLM2976OFR) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
Which are Natafort 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 GLYCOLS (UNII: 3WJQ0SDW1A)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- POVIDONE (UNII: FZ989GH94E)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- ETHYL VANILLIN (UNII: YC9ST449YJ)
- DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER (UNII: 905HNO1SIH)
What is the NDC to RxNorm Crosswalk for Natafort?
- RxCUI: 1304497 - alpha-tocopherol acetate 11 UNT / ascorbic acid 120 MG / cholecalciferol 400 UNT / folic acid 1 MG / iron carbonyl 60 MG / niacinamide 20 MG / pyridoxine hydrochloride 10 MG / riboflavin 3 MG / thiamine mononitrate 2 MG / vitamin B12 0.012 MG Oral Tablet
- RxCUI: 1304497 - alpha-tocopherol acetate 11 UNT / vitamin C 120 MG / cholecalciferol 400 UNT / folate 1 MG / iron carbonyl 60 MG / niacinamide 20 MG / vitamin B6 hydrochloride 10 MG / riboflavin 3 MG / vitamin B1 mononitrate 2 MG / vitamin B12 0.012 MG Oral Tablet
- RxCUI: 1304497 - alpha-tocopherol acetate 11 UNT / vitamin C 120 MG / cholecalciferol 400 UNT / folate 1 MG / iron carbonyl 60 MG / niacinamide 20 MG / vitamin B6 hydrochloride 10 MG / riboflavin 3 MG / vit-B1 mononitrate 2 MG / vitamin B12 0.012 MG Oral Tablet
- RxCUI: 1304497 - alpha-tocopherol acetate 11 UNT / vitamin C 120 MG / cholecalciferol 400 UNT / folate 1 MG / iron carbonyl 60 MG / niacinamide 20 MG / vit-B6 hydrochloride 10 MG / riboflavin 3 MG / vitamin B1 mononitrate 2 MG / vitamin B12 0.012 MG Oral Tablet
- RxCUI: 1304497 - alpha-tocopherol acetate 11 UNT / vitamin C 120 MG / cholecalciferol 400 UNT / folate 1 MG / iron carbonyl 60 MG / niacinamide 20 MG / vit-B6 hydrochloride 10 MG / riboflavin 3 MG / vit-B1 mononitrate 2 MG / vitamin B12 0.012 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".