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NDC 62756-0797-18 Divalproex Sodium 250 mg/1 Details
Divalproex Sodium 250 mg/1
Divalproex Sodium is a ORAL TABLET, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is DIVALPROEX SODIUM.
MedlinePlus Drug Summary
Valproic acid is used alone or with other medications to treat certain types of seizures. Valproic acid is also used to treat mania (episodes of frenzied, abnormally excited mood) in people with bipolar disorder (manic-depressive disorder; a disease that causes episodes of depression, episodes of mania, and other abnormal moods). It is also used to prevent migraine headaches but not to relieve headaches that have already begun. Valproic acid is in a class of medications called anticonvulsants. It works by increasing the amount of a certain natural substance in the brain.
Related Packages: 62756-0797-18Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Valproic Acid
Product Information
| NDC | 62756-0797 |
|---|---|
| Product ID | 62756-797_018d25b7-b6bb-4aad-809c-8fae51ed9fed |
| Associated GPIs | 72500010100610 |
| GCN Sequence Number | 004539 |
| GCN Sequence Number Description | divalproex sodium TABLET DR 250 MG ORAL |
| HIC3 | H4B |
| HIC3 Description | ANTICONVULSANTS |
| GCN | 17290 |
| HICL Sequence Number | 001884 |
| HICL Sequence Number Description | DIVALPROEX SODIUM |
| Brand/Generic | Generic |
| Proprietary Name | Divalproex Sodium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Divalproex Sodium |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, DELAYED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 250 |
| Active Ingredient Units | mg/1 |
| Substance Name | DIVALPROEX SODIUM |
| Labeler Name | Sun Pharmaceutical Industries, Inc. |
| Pharmaceutical Class | Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA078597 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 62756-0797-18 (62756079718)
| NDC Package Code | 62756-797-18 |
|---|---|
| Billing NDC | 62756079718 |
| Package | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-18) |
| Marketing Start Date | 2008-07-29 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |