NDC 71309-003-65 - Adult Low Dose
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
- 71309-003
- Requested NDC
- 71309-003-65
- Package NDCs from labels
- 71309-003-25, 71309-003-50, 71309-003-02, 71309-003-30, 71309-003-65, 71309-003-01, 71309-003-05, 71309-003-60, 71309-003-10
- Manufacturer
- Safrel Pharmaceuticals, LLC.
- Effective date
- 2023-03-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Aspirin 81 mg Enteric Coated Tablets | Safrel Pharmaceuticals, LLC. | 2023-03-28 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71309-003-01 | Adult Low Dose | 1000 in 1 BOTTLE | TABLET, DELAYED RELEASE | 1000 | 6 | |
| 71309-003-02 | Adult Low Dose | 2 in 1 POUCH | TABLET, DELAYED RELEASE | 2 | 6 | |
| 71309-003-05 | Adult Low Dose | 500 in 1 BOTTLE | TABLET, DELAYED RELEASE | 500 | 6 | |
| 71309-003-10 | Adult Low Dose | 1000 in 1 BOTTLE | TABLET, DELAYED RELEASE | 1000 | 6 | |
| 71309-003-25 | Adult Low Dose | 25 in 1 BOX | TABLET, DELAYED RELEASE | 25 | 6 | |
| 71309-003-25 | Adult Low Dose | 2 in 1 POUCH | TABLET, DELAYED RELEASE | 2 | 6 | |
| 71309-003-30 | Adult Low Dose | 30 in 1 BOTTLE | TABLET, DELAYED RELEASE | 30 | 6 | |
| 71309-003-30 | Adult Low Dose | 1 in 1 CARTON | TABLET, DELAYED RELEASE | 1 | 6 | |
| 71309-003-50 | Adult Low Dose | 50 in 1 BOX | TABLET, DELAYED RELEASE | 50 | 6 | |
| 71309-003-50 | Adult Low Dose | 2 in 1 POUCH | TABLET, DELAYED RELEASE | 2 | 6 | |
| 71309-003-60 | Adult Low Dose | 60 in 1 BOTTLE | TABLET, DELAYED RELEASE | 60 | 6 | |
| 71309-003-60 | Adult Low Dose | 1 in 1 CARTON | TABLET, DELAYED RELEASE | 1 | 6 | |
| 71309-003-65 | Adult Low Dose | 365 in 1 BOTTLE | TABLET, DELAYED RELEASE | 365 | 6 |
DailyMed Dashboard NDC Coverage#
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.