Divalproex Sodium
- Product NDC
- 0115-6911
- 11-digit product format
- 001156911
- Labeler code
- 0115
- Product ID
- 0115-6911_09f86269-2e96-4566-8618-b73baf128bcc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DIVALPROEX SODIUM
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Impax Generics
- Application
- ANDA078791
- Marketing category
- ANDA
- Marketing start
- 2009-08-04
- Marketing end
- 2019-10-31
- Substance
- DIVALPROEX SODIUM
- Active strength
- 250 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| b10a892b-b985-4cbc-9547-9ac4b72b784f | Product name | 2 | 20250818 |
| 7a3a03f1-382a-f9ec-0741-ff24dcbfed69 | Product name | 7 | 20250624 |
| 57fc3d01-4737-4091-9728-9e8a4c9e708d | Product name | 1 | 20200121 |
| 5d67ecc7-47c7-ec5e-e9eb-71bf00250645 | Product name | 1 | 20140508 |
| 97fce1a8-50c4-f088-0e31-64d82b6e9081 | Product name | 1 | 20140508 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0115-6911-01 | EA - Each | 0115-6911 | 278772b3-7ec8-4959-a1ea-7b34b53f05c5 | 1 | 2012-07-24 |
| 0115-6911-02 | EA - Each | 0115-6911 | b53c074c-0d8f-416e-92ac-5c518d1bcd0c | 1 | 2012-07-24 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1099563 | divalproex sodium 250 MG 24HR Extended Release Oral Tablet | PSN | 888fb978-ff34-1692-e053-2a95a90a25e0 | 8 |
| 1099563 | 24 HR divalproex sodium 250 MG Extended Release Oral Tablet | SCD | 888fb978-ff34-1692-e053-2a95a90a25e0 | 8 |
| 1099563 | divalproex sodium 250 MG 24 HR Extended Release Oral Tablet | SY | 888fb978-ff34-1692-e053-2a95a90a25e0 | 8 |