Depakote
- Product NDC
- 0074-6212
- 11-digit product format
- 000746212
- Labeler code
- 0074
- Product ID
- 0074-6212_7a9c5c8b-3192-4305-b360-ca106a4c85e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- AbbVie Inc.
- Application
- NDA018723
- Marketing category
- NDA
- Marketing start
- 1983-03-10
- Marketing end
- 2022-10-05
- Substance
- DIVALPROEX SODIUM
- Active strength
- 125 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 |
| 594e2c86-3079-4e6e-96c9-48f7a8afc78d | Product name | 1 | 20230718 |
| 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 Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0074-6212-13 | Depakote | 100 in 1 BOTTLE | TABLET, DELAYED RELEASE | 100 | 1621 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1099626 | Depakote 125 MG Delayed Release Oral Tablet | PSN | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099679 | Depakote 250 MG Delayed Release Oral Tablet | PSN | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099871 | Depakote 500 MG Delayed Release Oral Tablet | PSN | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099625 | divalproex sodium 125 MG Delayed Release Oral Tablet | PSN | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099678 | divalproex sodium 250 MG Delayed Release Oral Tablet | PSN | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099870 | divalproex sodium 500 MG Delayed Release Oral Tablet | PSN | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099626 | divalproex sodium 125 MG Delayed Release Oral Tablet [Depakote] | SBD | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099679 | divalproex sodium 250 MG Delayed Release Oral Tablet [Depakote] | SBD | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099871 | divalproex sodium 500 MG Delayed Release Oral Tablet [Depakote] | SBD | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099625 | divalproex sodium 125 MG Delayed Release Oral Tablet | SCD | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099678 | divalproex sodium 250 MG Delayed Release Oral Tablet | SCD | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099870 | divalproex sodium 500 MG Delayed Release Oral Tablet | SCD | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099626 | Depakote 125 MG Delayed Release Oral Tablet | SY | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099679 | Depakote 250 MG Delayed Release Oral Tablet | SY | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
| 1099871 | Depakote 500 MG Delayed Release Oral Tablet | SY | 08a65cf4-7749-4ceb-6895-8f4805e2b01f | 1621 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 0074-6212-13 | 00074621213 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0074-6212-13) | 1983-03-10 | 0000-00-00 | No | No | Current |