Estradiol
- Product NDC
- 70518-3922
- 11-digit product format
- 705183922
- Labeler code
- 70518
- Product ID
- 70518-3922_3ba3881f-2be9-c6fc-e063-6394a90a452d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estradiol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA217334
- Marketing category
- ANDA
- Marketing start
- 2023-11-22
- Substance
- ESTRADIOL
- Active strength
- 1 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Estradiol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ESTRADIOL | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4TI98Z838E |
| Rxcui | 197658 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-3922-0 | Estradiol | 30 in 1 BLISTER PACK | TABLET | 30 | | 5 |
| 70518-3922-1 | Estradiol | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3922 | ESTRADIOL TABLET [REMEDYREPACK INC.] | 4 | Current NDC, 2 package rows | 20250115_59a4b68d-a507-4809-a0c8-fd9799986d12.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-3922-0 | 70518392200 | 30 TABLET in 1 BLISTER PACK (70518-3922-0) | 30 tablet | 2023-11-22 | No | No | Current |
| 70518-3922-1 | 70518392201 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3922-1) | 90 tablet | 2025-01-13 | No | No | Current |