valproic

Generic: valproic acid

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valproic
Generic Name valproic acid
Labeler actavis pharma, inc.
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

valproic acid 250 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0591-4012
Product ID 0591-4012_a64ec7af-329d-4b8c-ad44-eedb68ec8f40
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073229
Listing Expiration 2026-12-31
Marketing Start 2009-09-08

Pharmacologic Class

Established (EPC)
anti-epileptic agent [epc] mood stabilizer [epc]
Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05914012
Hyphenated Format 0591-4012

Supplemental Identifiers

RxCUI
1099681
UNII
614OI1Z5WI
NUI
N0000175753 N0000008486 N0000175751

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name valproic (source: ndc)
Generic Name valproic acid (source: ndc)
Application Number ANDA073229 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0591-4012-01)
source: ndc

Packages (1)

0591-4012-01 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0591-4012-01)

Ingredients (1)

valproic acid (250 mg/1)

Linked Drug Pages (1)

Valproic ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a64ec7af-329d-4b8c-ad44-eedb68ec8f40", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751"], "unii": ["614OI1Z5WI"], "rxcui": ["1099681"], "spl_set_id": ["cef3e335-5891-412f-89c4-79fcd2f145b7"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]", "Mood Stabilizer [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0591-4012-01)", "package_ndc": "0591-4012-01", "marketing_start_date": "20090908"}], "brand_name": "Valproic", "product_id": "0591-4012_a64ec7af-329d-4b8c-ad44-eedb68ec8f40", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "0591-4012", "generic_name": "Valproic Acid", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valproic", "active_ingredients": [{"name": "VALPROIC ACID", "strength": "250 mg/1"}], "application_number": "ANDA073229", "marketing_category": "ANDA", "marketing_start_date": "20090908", "listing_expiration_date": "20261231"}