Estradiol
- Product NDC
- 68071-3689
- 11-digit product format
- 680713689
- Labeler code
- 68071
- Product ID
- 68071-3689_230c6613-46af-262a-e063-6394a90a121c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estradiol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA217334
- Marketing category
- ANDA
- Marketing start
- 2023-09-06
- 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 |
|---|
| 68071-3689-9 | 68071368909 | 100 TABLET in 1 BOTTLE (68071-3689-9) | 100 tablet | 2024-09-26 | No | No | Historical |