ella

Generic: ulipristal acetate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name ella
Generic Name ulipristal acetate
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ulipristal acetate 30 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5422
Product ID 50090-5422_cb78d0c3-de38-40ed-a74b-8391b860e1cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA022474
Listing Expiration 2026-12-31
Marketing Start 2020-05-11

Pharmacologic Class

Classes
progesterone agonist/antagonist [epc] selective progesterone receptor modulators [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905422
Hyphenated Format 50090-5422

Supplemental Identifiers

RxCUI
1005924 1005928
UNII
YF7V70N02B

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ella (source: ndc)
Generic Name ulipristal acetate (source: ndc)
Application Number NDA022474 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (50090-5422-0) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

ulipristal acetate (30 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cb78d0c3-de38-40ed-a74b-8391b860e1cb", "openfda": {"unii": ["YF7V70N02B"], "rxcui": ["1005924", "1005928"], "spl_set_id": ["e5f09468-7ac8-40ba-a85b-758a32f586c3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-5422-0)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "50090-5422-0", "marketing_start_date": "20210106"}], "brand_name": "Ella", "product_id": "50090-5422_cb78d0c3-de38-40ed-a74b-8391b860e1cb", "dosage_form": "TABLET", "pharm_class": ["Progesterone Agonist/Antagonist [EPC]", "Selective Progesterone Receptor Modulators [MoA]"], "product_ndc": "50090-5422", "generic_name": "ulipristal acetate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ella", "active_ingredients": [{"name": "ULIPRISTAL ACETATE", "strength": "30 mg/1"}], "application_number": "NDA022474", "marketing_category": "NDA", "marketing_start_date": "20200511", "listing_expiration_date": "20261231"}