Divalproex Sodium
- Product NDC
- 10370-511
- 11-digit product format
- 103700511
- Labeler code
- 10370
- Product ID
- 10370-511_a11aa682-1054-4905-84b0-e1b954f3c96b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA078445
- Marketing category
- ANDA
- Marketing start
- 2009-08-04
- Marketing end
- 2021-01-31
- 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
- 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 |
|---|---|---|---|---|---|
| 10370-511-10 | EA - Each | 10370-511 | 89274279-38e3-489c-9bd3-bf562a63d6cb | 1 | 2012-07-24 |
| 10370-511-50 | EA - Each | 10370-511 | 3e8b5e75-2af1-4cb9-a74a-eb12db68f9d0 | 1 | 2012-07-24 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1099569 | divalproex sodium 500 MG 24HR Extended Release Oral Tablet | PSN | 5a04842a-c10a-83ac-e053-2991aa0a0a42 | 1 |
| 1099569 | 24 HR divalproex sodium 500 MG Extended Release Oral Tablet | SCD | 5a04842a-c10a-83ac-e053-2991aa0a0a42 | 1 |
| 1099569 | divalproex sodium 500 MG 24 HR Extended Release Oral Tablet | SY | 5a04842a-c10a-83ac-e053-2991aa0a0a42 | 1 |