Divalproex sodium
- Product NDC
- 17856-0262
- 11-digit product format
- 178560262
- Labeler code
- 17856
- Product ID
- 17856-0262_e162e5fb-9963-4b11-85f6-8ea451da2964
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- ANDA209286
- Marketing category
- ANDA
- Marketing start
- 2020-09-18
- Marketing end
- 0000-00-00
- Substance
- DIVALPROEX SODIUM
- Active strength
- 500 1/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-0262-1 | Divalproex sodium | 100 in 1 BOX, UNIT-DOSE | TABLET, EXTENDED RELEASE | 100 | | 1 |
| 17856-0262-1 | Divalproex sodium | 1 in 1 POUCH | TABLET, EXTENDED RELEASE | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0262 | DIVALPROEX SODIUM TABLET, EXTENDED RELEASE [ATLANTIC BIOLOGICALS CORP.] | 1 | Legacy NDC, 2 package rows | 20211009_8697a048-a4d4-4934-a382-b73dba7f0cff.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17856-0262-1 | 17856026201 | 100 POUCH in 1 BOX, UNIT-DOSE (17856-0262-1) > 1 TABLET, EXTENDED RELEASE in 1 POUCH | 100 pouch | 2021-10-07 | 0000-00-00 | No | No | Current |