NDC 70518-3733-01 - Celecoxib
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
- 70518-3733
- Requested NDC
- 70518-3733-01
- Package NDCs from labels
- 70518-3733-0, 70518-3733-1, 70518-3733-2, 70518-3733-3, 70518-3733-4, 70518-3733-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-08-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Celecoxib - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-08-17 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-3733-0 | Celecoxib | 45 in 1 BOTTLE, PLASTIC | CAPSULE | 45 | 8 | |
| 70518-3733-1 | Celecoxib | 30 in 1 BOTTLE, PLASTIC | CAPSULE | 30 | 8 | |
| 70518-3733-2 | Celecoxib | 90 in 1 BOTTLE, PLASTIC | CAPSULE | 90 | 8 | |
| 70518-3733-3 | Celecoxib | 60 in 1 BOTTLE, PLASTIC | CAPSULE | 60 | 8 | |
| 70518-3733-4 | Celecoxib | 14 in 1 BOTTLE, PLASTIC | CAPSULE | 14 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-3733 | CELECOXIB CAPSULE [REMEDYREPACK INC.] | 6 | Current NDC, 5 package rows | 20241127_b3acbfd9-a1c2-4aa6-b5f0-013cfad6cca8.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70518-3733-1 | EA - Each | 70518-3733 | 56e63060-7338-47f9-bd29-a062f713650d | 1 | 2026-02-05 |
| 70518-3733-2 | EA - Each | 70518-3733 | 8e02b8d2-99d2-407c-919d-340c5dc16ec3 | 1 | 2026-02-05 |
| 70518-3733-3 | EA - Each | 70518-3733 | c73c1587-0319-41ae-9815-1746b29be135 | 1 | 2026-02-05 |
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 |
|---|---|---|---|---|---|---|
| Meijer Baby Tear Free SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Meijer Distributing Inc. | 2434de23-bcc9-4a83-9945-16fc3f2b8c61 | 2016-06-01 | Warnings | 15FIX9V2JP |
| TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted) | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE | Allergan, Inc. | 6a996e03-907f-4e6a-b232-0892b86956b0 | 2015-08-21 | Warnings | 15FIX9V2JP |
| Renewal Firming Day Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BURT'S BEES, INC. | 18ceb5d8-4b76-6a54-e054-00144ff88e88 | 2015-06-18 | Warnings | 15FIX9V2JP |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD. | 30468afc-9616-4765-b046-12e97a0a7827 | 2010-12-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.