NDC 70518-3822-01 - Naproxen
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
- 70518-3822
- Requested NDC
- 70518-3822-01
- Package NDCs from labels
- 70518-3822-0, 70518-3822-1, 70518-3822-2, 70518-3822-3, 70518-3822-4, 70518-3822-5, 70518-3822-6, 70518-3822-7, 70518-3822-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-06-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Naproxen - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-06-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-3822-0 | Naproxen | 30 in 1 BLISTER PACK | TABLET | 30 | 8 | |
| 70518-3822-1 | Naproxen | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | 8 | |
| 70518-3822-2 | Naproxen | 20 in 1 BOTTLE, PLASTIC | TABLET | 20 | 8 | |
| 70518-3822-3 | Naproxen | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | 8 | |
| 70518-3822-4 | Naproxen | 14 in 1 BOTTLE, PLASTIC | TABLET | 14 | 8 | |
| 70518-3822-5 | Naproxen | 6 in 1 BLISTER PACK | TABLET | 6 | 8 | |
| 70518-3822-6 | Naproxen | 28 in 1 BOTTLE, PLASTIC | TABLET | 28 | 8 | |
| 70518-3822-7 | Naproxen | 12 in 1 BOTTLE, PLASTIC | TABLET | 12 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-3822 | NAPROXEN TABLET [REMEDYREPACK INC.] | 7 | Current NDC, 8 package rows | 20241204_ccd95dfc-9236-4707-a715-6a12c91519ff.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70518-3822-1 | EA - Each | 70518-3822 | 0b97331a-046f-43a9-bf82-107d3c25e09c | 1 | 2026-01-08 |
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 |
|---|---|---|---|---|---|---|
| Naproxen | NAPROXEN | Cipla USA Inc. | e06c2b43-9882-442e-8413-10d9a33aecb9 | 2019-08-26 | Boxed warning, Warnings, Adverse reactions | 57Y76R9ATQ |
| NAPROXEN | NAPROXEN | TIME CAP LABORATORIES | 4350a2d9-5228-460e-b7b1-27e8fa846787 | 2018-10-09 | Warnings | 198014 198013 198012 57Y76R9ATQ |
| Naproxen | NAPROXEN | Aphena Pharma Solutions - Tennessee, LLC | e2347581-90da-429a-b17c-cffd0039fb86 | 2017-10-23 | Boxed warning, Warnings, Adverse reactions | 198014 198013 198012 57Y76R9ATQ |
| Naproxen | NAPROXEN | NCS HealthCare of KY, Inc dba Vangard Labs | 62a12771-bde9-4bc3-9ce9-672c8e31f020 | 2017-10-12 | Boxed warning, Warnings, Adverse reactions | 198014 57Y76R9ATQ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.