Divalproex Sodium D/R
- Product NDC
- 72189-636
- 11-digit product format
- 721890636
- Labeler code
- 72189
- Product ID
- 72189-636_3aff8f08-d8e9-cd13-e063-6394a90aa00c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium D/R
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA078597
- Marketing category
- ANDA
- Marketing start
- 2025-07-28
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Divalproex Sodium D/R
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIVALPROEX SODIUM | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 644VL95AO6 |
| Rxcui | 1099678 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-636-60 | Divalproex Sodium D/R | 60 in 1 BOTTLE | TABLET, DELAYED RELEASE | 60 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-636-60 | 72189063660 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-636-60) | 2025-07-28 | No | No | Historical |