NDC 50090-2835 Ella
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-2835 - Ella
Product Characteristics
Product Packages
NDC Code 50090-2835-0
Package Description: 1 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK
Product Details
What is NDC 50090-2835?
What are the uses for Ella?
Which are Ella UNII Codes?
The UNII codes for the active ingredients in this product are:
- ULIPRISTAL ACETATE (UNII: YF7V70N02B)
- ULIPRISTAL (UNII: 6J5J15Q2X8) (Active Moiety)
Which are Ella 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- POVIDONE K30 (UNII: U725QWY32X)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Ella?
- RxCUI: 1005924 - ulipristal acetate 30 MG Oral Tablet
- RxCUI: 1005928 - Ella 30 MG Oral Tablet
- RxCUI: 1005928 - ulipristal acetate 30 MG Oral Tablet [Ella]
* Please review the disclaimer below.
Patient Education
Ulipristal
Ulipristal is used to prevent pregnancy after unprotected sexual intercourse (sex without any method of birth control or with a birth control method that failed or was not used properly [e.g., a condom that slipped or broke or birth control pills that were not taken as scheduled]). Ulipristal should not be used to prevent pregnancy on a regular basis. This medication is to be used as an emergency contraceptive or backup in case regular birth control fails or is used incorrectly. Ulipristal is in a class of medications called progestins. It works by preventing or delaying the release of an egg from the ovary. It also may work by changing the lining of the uterus (womb) to prevent development of a pregnancy. Ulipristal may prevent pregnancy, but it will not prevent the spread of human immunodeficiency virus (HIV, the virus that causes acquired immunodeficiency syndrome [AIDS]) and other sexually transmitted diseases.
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* 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".