estrogens, conjugated
- Product NDC
- 50742-390
- 11-digit product format
- 507420390
- Labeler code
- 50742
- Product ID
- 50742-390_11c5dbc7-30bb-482c-bac7-4c94b72c44ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- estrogens, conjugated
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA214023
- Marketing category
- ANDA
- Marketing start
- 2025-10-16
- Substance
- ESTROGENS, CONJUGATED
- Active strength
- .9 mg/1
- Pharmacologic classes
- Estrogen Receptor Agonists [MoA], Estrogen [EPC], Estrogens, Conjugated (USP) [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- estrogens, conjugated
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ESTROGENS, CONJUGATED | .9 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | IU5QR144QX |
| Rxcui | 197661, 197662 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50742-390-01 | estrogens, conjugated | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 1 |
| 50742-390-10 | estrogens, conjugated | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50742-390-01 | 50742039001 | 100 TABLET, FILM COATED in 1 BOTTLE (50742-390-01) | 2025-10-16 | No | No | Historical |
| 50742-390-10 | 50742039010 | 1000 TABLET, FILM COATED in 1 BOTTLE (50742-390-10) | 2025-10-16 | No | No | Historical |