NDC 57297-903 Kaitlib Fe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BROWN (C48332)
LU;I62
Code Structure Chart
Product Details
What is NDC 57297-903?
What are the uses for Kaitlib Fe?
Which are Kaitlib Fe UNII Codes?
The UNII codes for the active ingredients in this product are:
- NORETHINDRONE (UNII: T18F433X4S)
- NORETHINDRONE (UNII: T18F433X4S) (Active Moiety)
- ETHINYL ESTRADIOL (UNII: 423D2T571U)
- ETHINYL ESTRADIOL (UNII: 423D2T571U) (Active Moiety)
Which are Kaitlib Fe 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:
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- POVIDONE K30 (UNII: U725QWY32X)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- VANILLIN (UNII: CHI530446X)
- FERROUS FUMARATE (UNII: R5L488RY0Q)
What is the NDC to RxNorm Crosswalk for Kaitlib Fe?
- RxCUI: 1095223 - ferrous fumarate 75 MG Chewable Tablet
- RxCUI: 1099638 - ethinyl estradiol 0.025 MG / norethindrone 0.8 MG Chewable Tablet
- RxCUI: 1099638 - ethinyl estradiol 25 MCG / norethindrone 0.8 MG Chewable Tablet
- RxCUI: 1607990 - {24 (ethinyl estradiol 0.025 MG / norethindrone 0.8 MG Chewable Tablet) / 4 (ferrous fumarate 75 MG Chewable Tablet) } Pack
- RxCUI: 1607990 - Eth estra-Noreth 0.025-0.8 MG (24) Chewable Tablet / Ferr fum 75 MG (4) Chewable Tablet 28 Day Pack
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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".