Estradiol
- Product NDC
- 70518-3910
- 11-digit product format
- 705183910
- Labeler code
- 70518
- Product ID
- 70518-3910_3ba1a9f8-7c95-f6bd-e063-6394a90aa499
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estradiol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA217334
- Marketing category
- ANDA
- Marketing start
- 2023-11-07
- Substance
- ESTRADIOL
- Active strength
- 2 mg/1
- Pharmacologic classes
- Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4TI98Z838E | ESTRADIOL | 50-28-2 | ESTRADIOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-3910-2 | 70518391002 | 30 TABLET in 1 BLISTER PACK (70518-3910-2) | 30 tablet | 2023-11-10 | No | No | Historical |