Divalproex Sodium
- Product NDC
- 0904-6860
- 11-digit product format
- 009046860
- Labeler code
- 0904
- Product ID
- 0904-6860_946b4453-7cb3-4bb5-b9ca-cdf732af2ca0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA078597
- Marketing category
- ANDA
- Marketing start
- 2008-07-29
- 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
- 2026-12-31
- Current FDA listing
- Yes
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 |
| fb7ab793-2c12-4079-b100-a64f73bef25a | Product name | 4 | 20240712 |
| b0cbf770-6cc3-4aa4-9158-755110c2b9f7 | Product name | 2 | 20230717 |
| dc7c5daa-021f-40dd-b00d-63982cb2067a | Product name | 1 | 20230426 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 5 | 20200925 |
| 57fc3d01-4737-4091-9728-9e8a4c9e708d | Product name | 1 | 20200121 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 2 | 20160823 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
| 5d67ecc7-47c7-ec5e-e9eb-71bf00250645 | Product name | 1 | 20140508 |
| 97fce1a8-50c4-f088-0e31-64d82b6e9081 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0904-6860-61 | Divalproex Sodium | 100 in 1 CARTON | TABLET, DELAYED RELEASE | 100 | 8 | |
| 0904-6860-61 | Divalproex Sodium | 1 in 1 BLISTER PACK | TABLET, DELAYED RELEASE | 1 | 8 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0904-6860-61 | EA - Each | 0904-6860 | 58762e09-2c3b-4993-a271-c27088b08803 | 1 | 2019-09-05 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1099678 | divalproex sodium 250 MG Delayed Release Oral Tablet | PSN | fb39a94e-93e6-4afe-a300-f80e8f1e0fa6 | 8 |
| 1099870 | divalproex sodium 500 MG Delayed Release Oral Tablet | PSN | fb39a94e-93e6-4afe-a300-f80e8f1e0fa6 | 8 |
| 1099678 | divalproex sodium 250 MG Delayed Release Oral Tablet | SCD | fb39a94e-93e6-4afe-a300-f80e8f1e0fa6 | 8 |
| 1099870 | divalproex sodium 500 MG Delayed Release Oral Tablet | SCD | fb39a94e-93e6-4afe-a300-f80e8f1e0fa6 | 8 |
| 1099678 | divalproex sodium 250 MG Delayed Release Oral Tablet | PSN | 5e59609f-d79d-414b-a6fc-7efb1ba5b200 | 7 |
| 1099870 | divalproex sodium 500 MG Delayed Release Oral Tablet | PSN | 5e59609f-d79d-414b-a6fc-7efb1ba5b200 | 7 |
| 1099678 | divalproex sodium 250 MG Delayed Release Oral Tablet | SCD | 5e59609f-d79d-414b-a6fc-7efb1ba5b200 | 7 |
| 1099870 | divalproex sodium 500 MG Delayed Release Oral Tablet | SCD | 5e59609f-d79d-414b-a6fc-7efb1ba5b200 | 7 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0904-6860-61 | 00904686061 | 100 BLISTER PACK in 1 CARTON (0904-6860-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | 100 blister pack | 2008-07-29 | 0000-00-00 | No | No | Current |