NDC 0310-1110-01 - LOKELMA
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
- 0310-1110
- Requested NDC
- 0310-1110-01
- Package NDCs from labels
- 0310-1110-01, 0310-1110-30, 0310-1110-91, 0310-1110-98, 0310-1110-39, 0310-1110-94, 0310-1110-93
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2026-03-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| LOKELMA - A-S Medication Solutions | A-S Medication Solutions | 2026-03-26 | HUMAN PRESCRIPTION DRUG LABEL |
| LOKELMA - AstraZeneca Pharmaceuticals LP | AstraZeneca PLC | AstraZeneca Pharmaceuticals LP | AstraZeneca PLC | 2024-02-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0310-1110-01 | LOKELMA | 10 g in 1 PACKET | POWDER, FOR SUSPENSION | 10 | 28 | |
| 0310-1110-30 | LOKELMA | 30 in 1 BOX | POWDER, FOR SUSPENSION | 30 | 28 | |
| 0310-1110-39 | LOKELMA | 11 in 1 BOX | POWDER, FOR SUSPENSION | 11 | 28 | |
| 0310-1110-91 | LOKELMA | 10 g in 1 PACKET | POWDER, FOR SUSPENSION | 10 | 28 | |
| 0310-1110-93 | LOKELMA | 3 in 1 BOX | POWDER, FOR SUSPENSION | 3 | 28 | |
| 0310-1110-94 | LOKELMA | 11 in 1 BOX | POWDER, FOR SUSPENSION | 11 | 28 | |
| 0310-1110-98 | LOKELMA | 30 in 1 BOX | POWDER, FOR SUSPENSION | 30 | 28 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0310-1110-01 | EA - Each | 0310-1110 | 5fc5445c-17d1-4c7c-ad80-106fa61cde7f | 1 | 2018-09-05 |
| 0310-1110-30 | EA - Each | 0310-1110 | ce05dd26-736f-46d9-90ec-a012ccb6ea30 | 1 | 2018-09-05 |
| 0310-1110-39 | EA - Each | 0310-1110 | bf60586d-683d-439e-8a6f-5a8df3ae5624 | 1 | 2018-12-13 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| LOKELMA | SODIUM ZIRCONIUM CYCLOSILICATE | A-S Medication Solutions | 8833d6e6-33ab-4ea9-b78f-3ec30a904ef8 | 2026-03-26 | Warnings, Adverse reactions | NDA207078 50090-6501-1 50090-6501-0 50090-6501 2053927 2047642 5bb5ae7d-0be6-4ecc-bb31-4eedd2f724b9 8833d6e6-33ab-4ea9-b78f-3ec30a904ef8 D652ZWF066 |
| LOKELMA | SODIUM ZIRCONIUM CYCLOSILICATE | AstraZeneca Pharmaceuticals LP | 90bf8e28-748d-4e4b-a19f-9cf483370eff | 2024-02-08 | Warnings, Adverse reactions | NDA207078 0310-1110-93 0310-1110-98 0310-1110-91 0310-1105-39 0310-1110-01 0310-1110-39 0310-1110-30 0310-1105-30 0310-1110-94 0310-1105-01 0310-1110 0310-1105 00310111001 2053927 2047639 2047642 2047633 e97b97a9-6ad1-4b47-a5be-fefd7be47c23 90bf8e28-748d-4e4b-a19f-9cf483370eff D652ZWF066 |
| LOKELMA | SODIUM ZIRCONIUM CYCLOSILICATE | A-S Medication Solutions | 7f7ed64d-8480-4143-a207-29c24a0b9363 | 2023-05-31 | Warnings, Adverse reactions | NDA207078 2047639 2047633 D652ZWF066 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.