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NDC 17856-0792-06 Valproic Acid 250 mg/5mL Details
Valproic Acid 250 mg/5mL
Valproic Acid is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ATLANTIC BIOLOGICALS CORP.. The primary component is VALPROIC ACID.
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: 17856-0792-06Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Valproic Acid
Product Information
| NDC | 17856-0792 |
|---|---|
| Product ID | 17856-0792_b291ea1d-42fe-4c43-a13a-97f6e53724d9 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Valproic Acid |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Valproic Acid |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | SOLUTION |
| Route | ORAL |
| Active Ingredient Strength | 250 |
| Active Ingredient Units | mg/5mL |
| Substance Name | VALPROIC ACID |
| Labeler Name | ATLANTIC BIOLOGICALS CORP. |
| 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 | ANDA074060 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 17856-0792-06 (17856079206)
| NDC Package Code | 17856-0792-6 |
|---|---|
| Billing NDC | 17856079206 |
| Package | 72 CUP in 1 BOX, UNIT-DOSE (17856-0792-6) / 5 mL in 1 CUP (17856-0792-5) |
| Marketing Start Date | 2023-02-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |