NDC 70518-2104-2 - topiramate
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
- 70518-2104
- Requested NDC
- 70518-2104-2
- Package NDCs from labels
- 70518-2104-0, 70518-2104-2, 70518-2104-1, 70518-2104-3, 70518-2104-4, 70518-2104-6, 70518-2104-5, 70518-2104-7, 70518-2104-8, 70518-2104-9
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-07-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| topiramate - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-07-17 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-2104-0 | topiramate | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | 19 | |
| 70518-2104-1 | topiramate | 30 in 1 BOX | TABLET, FILM COATED | 30 | 19 | |
| 70518-2104-2 | topiramate | 1 in 1 POUCH | TABLET, FILM COATED | 1 | 19 | |
| 70518-2104-3 | topiramate | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 60 | 19 | |
| 70518-2104-4 | topiramate | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | 19 | |
| 70518-2104-5 | topiramate | 100 in 1 BOX | TABLET, FILM COATED | 100 | 19 | |
| 70518-2104-6 | topiramate | 1 in 1 POUCH | TABLET, FILM COATED | 1 | 19 | |
| 70518-2104-7 | topiramate | 28 in 1 BLISTER PACK | TABLET, FILM COATED | 28 | 19 | |
| 70518-2104-8 | topiramate | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | 19 | |
| 70518-2104-9 | topiramate | 180 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 180 | 19 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-2104 | TOPIRAMATE TABLET, FILM COATED [REMEDYREPACK INC.] | 13 | Current NDC, Legacy NDC, 10 package rows | 20250306_7e0834ee-920b-496f-954d-f9d81c3ba2d6.zip |
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 |
|---|---|---|---|---|---|---|
| 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.