United States · FDA National Drug Code directory
Ella
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 73302-456_30e0d760-1e27-456f-8420-ad1c219f49f7
- Product NDC
- 73302-456
- Form
- TABLET
- Composition / generic term
- ulipristal acetate
- Labeler
- PMI Branded Pharmaceuticals, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20200511
- Source listing expiry
- 20271231
Source-listed ingredients
- ULIPRISTAL ACETATE — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (73302-456-01) / 1 TABLET in 1 BLISTER PACK · 73302-456-01
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →