Divalproex Sodium
- Product NDC
- 64679-725
- 11-digit product format
- 646790725
- Labeler code
- 64679
- Product ID
- 64679-725_1ba11532-9a82-4c2d-9679-c771dab78926
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA078705
- Marketing category
- ANDA
- Marketing start
- 2009-08-04
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64679-725 | DIVALPROEX SODIUM ER (DIVALPROEX SODIUM) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT USA LLC.] | 6 | Legacy NDC | 20201219_a93b0914-c1ac-4e48-b6b9-1b4e211eb072.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64679-725-01 | 64679072501 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-725-01) | | 2009-08-04 | 0000-00-00 | No | No | Current |
| 64679-725-02 | 64679072502 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-725-02) | | 2009-08-04 | 0000-00-00 | No | No | Current |
| 64679-725-03 | 64679072503 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-725-03) | | 2009-08-04 | 0000-00-00 | No | No | Current |
| 64679-725-04 | 64679072504 | 10 BLISTER PACK in 1 CARTON (64679-725-04) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 2009-08-04 | 0000-00-00 | No | No | Current |