NDC 70518-3597-01 - Pregabalin
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
- 70518-3597
- Requested NDC
- 70518-3597-01
- Package NDCs from labels
- 70518-3597-0, 70518-3597-1, 70518-3597-2, 70518-3597-3, 70518-3597-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-08-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Pregabalin - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-08-14 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-3597-0 | Pregabalin | 90 in 1 BOTTLE, PLASTIC | CAPSULE | 90 | 8 | |
| 70518-3597-1 | Pregabalin | 60 in 1 BOTTLE, PLASTIC | CAPSULE | 60 | 8 | |
| 70518-3597-2 | Pregabalin | 90 in 1 BOTTLE, PLASTIC | CAPSULE | 90 | 8 | |
| 70518-3597-3 | Pregabalin | 60 in 1 BOTTLE, PLASTIC | CAPSULE | 60 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-3597 | PREGABALIN CAPSULE [REMEDYREPACK INC.] | 5 | Current NDC, Legacy NDC, 4 package rows | 20241218_12309847-0857-4ff7-a7e7-edeadc3dfb61.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70518-3597-0 | EA - Each | 70518-3597 | d1f128c7-0e21-4032-9628-d267b2b46f42 | 1 | 2026-01-08 |
| 70518-3597-1 | EA - Each | 70518-3597 | 05f433e5-ae15-499d-a974-444416d59606 | 1 | 2026-01-08 |
| 70518-3597-2 | EA - Each | 70518-3597 | e26c2135-c861-4292-b7bd-4dd8ecd006e6 | 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 |
|---|---|---|---|---|---|---|
| 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.