Divalproex sodium
- Product NDC
- 70518-1897
- 11-digit product format
- 705181897
- Labeler code
- 70518
- Product ID
- 70518-1897_c50ac22f-7a07-b662-e053-2995a90a4d10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex sodium
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202419
- Marketing category
- ANDA
- Marketing start
- 2019-02-22
- Marketing end
- 0000-00-00
- Substance
- DIVALPROEX SODIUM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1897 | DIVALPROEX SODIUM TABLET, FILM COATED, EXTENDED RELEASE [REMEDYREPACK INC.] | 12 | Legacy NDC | 20240907_66b0a3e0-70df-469e-845f-17769482304b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1897-0 | 70518189700 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-1897-0) | | 2019-02-22 | 0000-00-00 | No | No | Current |
| 70518-1897-1 | 70518189701 | 100 POUCH in 1 BOX, UNIT-DOSE (70518-1897-1) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-1897-2) | 100 pouch | 2019-10-17 | 0000-00-00 | No | No | Current |