NDC 17856-4012
Valproic
Valproic Acid
Valproic is a Oral Capsule, Liquid Filled in the Human Prescription Drug category. It is labeled and distributed by Atlantic Biologicals Corp.. The primary component is Valproic Acid.
| Product ID | 17856-4012_c083ff59-eb2c-46d0-8be0-b19d11776c09 |
| NDC | 17856-4012 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Valproic |
| Generic Name | Valproic Acid |
| Dosage Form | Capsule, Liquid Filled |
| Route of Administration | ORAL |
| Marketing Start Date | 2009-09-08 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA073229 |
| Labeler Name | ATLANTIC BIOLOGICALS CORP. |
| Substance Name | VALPROIC ACID |
| Active Ingredient Strength | 250 mg/1 |
| Pharm Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |