NDC 65862-709-10 - Raloxifene Hydrochloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 65862-709
- Requested NDC
- 65862-709-10
- Package NDCs from labels
- 65862-709-30, 65862-709-01, 65862-709-22, 65862-709-10, 65862-709-03, 65862-709-99
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2025-11-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Raloxifene Hydrochloride - A-S Medication Solutions | A-S Medication Solutions | 2025-11-06 | Human Prescription Drug Label |
| Raloxifene Hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-04-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Raloxifene Hydrochloride - Aurobindo Pharma Limited | Aurobindo Pharma Limited | 2024-02-17 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 65862-709-01 | Raloxifene Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 7 | |
| 65862-709-03 | Raloxifene Hydrochloride | 3 in 1 CARTON | TABLET, FILM COATED | 3 | 7 | |
| 65862-709-10 | Raloxifene Hydrochloride | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 7 | |
| 65862-709-22 | Raloxifene Hydrochloride | 2000 in 1 BOTTLE | TABLET, FILM COATED | 2000 | 7 | |
| 65862-709-30 | Raloxifene Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 7 | |
| 65862-709-99 | Raloxifene Hydrochloride | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 7 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 65862-709-01 | EA - Each | 65862-709 | 1fbb9680-3188-4851-90d6-5d0eeccf881f | 1 | 2021-05-05 |
| 65862-709-30 | EA - Each | 65862-709 | d5df931c-abb5-4c2a-8f3b-4340042bd169 | 1 | 2021-11-09 |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.