Divalproex sodium 250 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 70518-4557-00 |
|---|---|
| Product NDC | 70518-4557 |
| Generic Drug Name | divalproex sodium |
| Brand Name | divalproex sodium |
| Manufacturer | Remedyrepack Inc. |
| Strength | 250 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 30 Tablet, Film Coated, Extended Release |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4557-0) |
| Active Ingredients | Divalproex Sodium |
| Marketing Category | ANDA |
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NDC snapshot
divalproex sodium 250 mg / 1 Tablet is tracked under NDC 70518-4557-00 and rolls up into product family 70518-4557. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.
- Package configuration: 30 Tablet, Film Coated, Extended Release.
- Manufacturer: Remedyrepack Inc..
- Dosage form: Tablet.
- Family size: 1 indexed presentation.
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Official references
Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.
Divalproex sodium 250 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release, NDC 70518-4557-00, is a Remedyrepack Inc. 250 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated, Extended Release.
NDC search formats
- Canonical NDC 11: 70518-4557-00
- Digits-only NDC 11: 70518455700
- Possible 10-digit display format: 70518-4557-0 (7051845570)
Helpful product links
- Search by brand name: divalproex sodium
- Exact NDC 11: 70518-4557-00
- Product family NDC: 70518-4557
