Divalproex Sodium
- Product NDC
- 68151-1164
- 11-digit product format
- 681511164
- Labeler code
- 68151
- Product ID
- 68151-1164_eb8df045-1d10-4de4-bf33-d29e36400eca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA078597
- Marketing category
- ANDA
- Marketing start
- 2008-07-29
- Marketing end
- 0000-00-00
- 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
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-1164-8 | Divalproex Sodium | 1 in 1 PACKAGE | TABLET, DELAYED RELEASE | 1 | | 4 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| DIVALPROEX SODIUM | ACTIVE INGREDIENT | 644VL95AO6 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| VALPROIC ACID | ACTIVE MOIETY | 614OI1Z5WI | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A | INACTIVE INGREDIENT | NX76LV5T8J | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| POVIDONE K30 | INACTIVE INGREDIENT | U725QWY32X | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| SODIUM BICARBONATE | INACTIVE INGREDIENT | 8MDF5V39QO | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| TRIACETIN | INACTIVE INGREDIENT | XHX3C3X673 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| TRIETHYL CITRATE | INACTIVE INGREDIENT | 8Z96QXD6UM | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-1164 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT] | 4 | Legacy NDC, 1 package rows | 20170706_ba88eafe-b773-4c41-aa80-be86e799cc86.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-1164-8 | 68151116408 | 1 in 1 PACKAGE | Historical |