Ella
- Product NDC
- 73302-456
- 11-digit product format
- 733020456
- Labeler code
- 73302
- Product ID
- 73302-456_47d0b808-7143-c7a9-e063-6394a90a6e0d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ulipristal acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- HRA PHARMA AMERICA, INC.
- Application
- NDA022474
- Marketing category
- NDA
- Marketing start
- 2020-05-11
- Substance
- ULIPRISTAL ACETATE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Progesterone Agonist/Antagonist [EPC], Selective Progesterone Receptor Modulators [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ella
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ULIPRISTAL ACETATE | 30 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YF7V70N02B |
| Rxcui | 1005924, 1005928 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73302-456-01 | Ella | 1 in 1 CARTON | TABLET | 1 | | 6 |
| 73302-456-01 | Ella | 1 in 1 BLISTER PACK | TABLET | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73302-456 | ELLA (ULIPRISTAL ACETATE) TABLET [HRA PHARMA AMERICA, INC.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20250202_2bf93d23-cddd-4613-9066-5b5fa090404b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73302-456-01 | 73302045601 | 1 BLISTER PACK in 1 CARTON (73302-456-01) / 1 TABLET in 1 BLISTER PACK | 1 blister pack | 2020-05-11 | 0000-00-00 | No | No | Current |