NDC 70518-3055-2 - Divalproex Sodium
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
- 70518-3055
- Requested NDC
- 70518-3055-2
- Package NDCs from labels
- 70518-3055-0, 70518-3055-2, 70518-3055-1, 70518-3055-4, 70518-3055-3, 70518-3055-5, 70518-3055-6, 70518-3055-7
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-07-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Divalproex Sodium - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-07-21 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-3055-0 | Divalproex Sodium | 30 in 1 BLISTER PACK | TABLET, DELAYED RELEASE | 30 | 15 | |
| 70518-3055-1 | Divalproex Sodium | 100 in 1 BOX | TABLET, DELAYED RELEASE | 100 | 15 | |
| 70518-3055-2 | Divalproex Sodium | 1 in 1 POUCH | TABLET, DELAYED RELEASE | 1 | 15 | |
| 70518-3055-3 | Divalproex Sodium | 100 in 1 BOX | TABLET, DELAYED RELEASE | 100 | 15 | |
| 70518-3055-4 | Divalproex Sodium | 1 in 1 POUCH | TABLET, DELAYED RELEASE | 1 | 15 | |
| 70518-3055-5 | Divalproex Sodium | 60 in 1 BLISTER PACK | TABLET, DELAYED RELEASE | 60 | 15 | |
| 70518-3055-6 | Divalproex Sodium | 30 in 1 BLISTER PACK | TABLET, DELAYED RELEASE | 30 | 15 | |
| 70518-3055-7 | Divalproex Sodium | 30 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 30 | 15 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-3055 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [REMEDYREPACK INC.] | 11 | Current NDC, Legacy NDC, 8 package rows | 20250214_5926c3ff-c995-4789-941c-d38aa7db94dc.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70518-3055-0 | EA - Each | 70518-3055 | 302b9247-c6e7-4df0-9eb8-41615cfe0c2e | 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 |
|---|---|---|---|---|---|---|
| Droptics Performance Eye Drops | NAPHAZOLINE HYDROCHLORIDE, PROPYLENE GLYCOL | Droptics LLC | 20fd6822-a7fd-4593-92bb-0a07260893e2 | 2026-02-09 | Warnings | 6DC9Q167V3 |
| Youmi Alcohol Prep Pad 70 Isopropyl Alcohol | ISOPROPYL ALCOHOL | PT YOUMI MEDIKA INDUSTRI | e3b1a576-a8eb-44bf-8f9c-a49a44a894e8 | 2026-02-09 | Warnings | ND2M416302 |
| EVERLIT CARE PRODUCTS PREP PAD | ISOPROPYL ALCOHOL | EVERLIT GLOBAL INC. | 77a60360-8bb5-43e9-b7e4-f71d2d488c44 | 2026-02-09 | Warnings | ND2M416302 |
| Everlit Care Products Sting Relief | ISOPROPYL ALCOHOL | EVERLIT GLOBAL INC. | adfab206-b7de-4f6a-a864-edd946ea743d | 2026-02-09 | Warnings | ND2M416302 |
| Mold, Yeast and Dust | ADRENALINUM, ARSENICUM IODATUM, ASPERGILLUS FLAVUS, ASPERGILLUS FUMIGATUS, ASPERGILLUS GLAUCUS, ASPERGILLUS NIDULANS, ASPERGILLUS NIGER, CANDIDA ALBICANS, DERMATOPHAGOIDES FARINAE, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, MUCOR PLUMBEUS, NATRUM SULPHURICUM, PENICILLIUM DIGITATUM, PENICILLIUM ROQUEFORTII, SACCHAROMYCES CEREVISIAE, SILICEA | NaturalCare | 32afa0f0-bca5-4246-bc2e-decd757fcf9d | 2026-02-09 | Warnings | ETJ7Z6XBU4 |
| Alcohol | ISOPROPYL ALCOHOL | A-S Medication Solutions | 6b8834be-0235-4f7c-8d52-c2f6aa2d3049 | 2026-02-08 | Warnings | ND2M416302 |
| Hampton Sun SPF 50 Mineral | ZINC OXIDE 19.5% TITANIUM DIOXIDE 4.00% | S&C Hampton Sun LLC | d6c33436-042e-44e8-8b55-98be6e246879 | 2026-02-06 | Warnings | 15FIX9V2JP |
| SHISEIDO WASO COLOR-SMART DAY MOISTURIZER | OCTINOXATE, TITANIUM DIOXIDE | Shiseido Americas Corporation | f291f077-1c72-48fc-bb19-c20bdeaaa596 | 2026-02-06 | Warnings | 15FIX9V2JP |
| SHISEIDO WASO COLOR-SMART DAY MOISTURIZER | OCTINOXATE, TITANIUM DIOXIDE | Shiseido Americas Corporation | 54f63dd8-e77f-42e4-a6d3-61ab7beecf50 | 2026-02-06 | Warnings | 15FIX9V2JP |
| SEYTU Body Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Omnilife USA, Inc. | c411e9a6-b2ea-446b-a886-b92c61736e6c | 2026-02-05 | Warnings | 15FIX9V2JP |
| SEYTU Facial Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Omnilife USA, Inc. | 96fd37fb-c3ff-413f-b2c8-50754f320ecc | 2026-02-05 | Warnings | 15FIX9V2JP |
| 70% Rubbing | ISOPROPYL ALCOHOL | Walgreens Co. | 6ad37d18-5c19-4b5f-8313-edd430f84fb0 | 2026-02-05 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Walgreens Co. | 1473e6e4-dc5f-43d9-a249-111a181e3f76 | 2026-02-05 | Warnings, Adverse reactions | ND2M416302 |
| ForPro Premium Sterile Antiseptic Isopropyl Alcohol Pads | ISOPROPYL ALCOHOL | Tng workdwide | 6cc2ccae-b288-473e-a736-0974c96dbb89 | 2026-02-05 | Warnings | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Pharmacy Value Alliance, LLC | 528011d7-8c6d-4940-bee1-52b39acef40d | 2026-02-05 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Publix Super Markets, Inc. | 14aecc7b-c68a-4cb9-863f-475e204f66a5 | 2026-02-05 | Warnings | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Publix Super Markets, Inc. | b3b5324b-ee2c-4f87-9bb9-81d3d85f73ee | 2026-02-05 | Warnings | ND2M416302 |
| No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Bamboo | OCTINOXATE, TITANIUM DIOXIDE | BCM Cosmetique SAS | ebfe03e7-614f-44b1-b1f1-78edc7e274cc | 2026-02-05 | Warnings | 15FIX9V2JP |
| Isopropyl alcohol 50 percent | ISOPROPYL ALCOHOL | EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC) | b1b52183-3296-48b2-b3d3-821c141b0bea | 2026-02-05 | Warnings | ND2M416302 |
| Isopropyl alcohol 50 percent | ISOPROPYL ALCOHOL | EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC) | ee67fb96-fa2c-4542-8fdb-f2ccd885ee53 | 2026-02-05 | Warnings | ND2M416302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.