NDC 57297-857 Levonorgestrel And Ethinyl Estradiol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
WHITE (C48325 - WHITE TO OFF WHITE)
PINK (C48328)
ORANGE (C48331)
LU;W32
LU;W33
LU;T22
Code Structure Chart
Product Details
What is NDC 57297-857?
Which are Levonorgestrel And Ethinyl Estradiol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ETHINYL ESTRADIOL (UNII: 423D2T571U)
- ETHINYL ESTRADIOL (UNII: 423D2T571U) (Active Moiety)
- LEVONORGESTREL (UNII: 5W7SIA7YZW)
- LEVONORGESTREL (UNII: 5W7SIA7YZW) (Active Moiety)
Which are Levonorgestrel And Ethinyl Estradiol 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- STARCH, CORN (UNII: O8232NY3SJ)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Levonorgestrel And Ethinyl Estradiol?
- RxCUI: 310230 - ethinyl estradiol 0.03 MG / levonorgestrel 0.05 MG Oral Tablet
- RxCUI: 348804 - ethinyl estradiol 0.03 MG / levonorgestrel 0.125 MG Oral Tablet
- RxCUI: 348804 - ethinyl estradiol 30 MCG / levonorgestrel 125 MCG Oral Tablet
- RxCUI: 348805 - ethinyl estradiol 0.04 MG / levonorgestrel 0.075 MG Oral Tablet
- RxCUI: 348805 - ethinyl estradiol 40 MCG / levonorgestrel 75 MCG Oral Tablet
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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".