valproic acid

Generic: valproic acid

Labeler: ani pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valproic acid
Generic Name valproic acid
Labeler ani pharmaceuticals, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

valproic acid 250 mg/5mL

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 62559-266
Product ID 62559-266_5087247f-33a7-4dec-8a0b-f79e80f7debd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073178
Listing Expiration 2026-12-31
Marketing Start 2024-01-02

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 62559266
Hyphenated Format 62559-266

Supplemental Identifiers

RxCUI
1099687
UPC
0362559266161
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 acid (source: ndc)
Generic Name valproic acid (source: ndc)
Application Number ANDA073178 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (62559-266-16)
source: ndc

Packages (1)

Ingredients (1)

valproic acid (250 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5087247f-33a7-4dec-8a0b-f79e80f7debd", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751"], "upc": ["0362559266161"], "unii": ["614OI1Z5WI"], "rxcui": ["1099687"], "spl_set_id": ["2314af65-b928-42a9-91eb-6372909ab4f5"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]", "Mood Stabilizer [EPC]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (62559-266-16)", "package_ndc": "62559-266-16", "marketing_start_date": "20240102"}], "brand_name": "Valproic Acid", "product_id": "62559-266_5087247f-33a7-4dec-8a0b-f79e80f7debd", "dosage_form": "SOLUTION", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "62559-266", "generic_name": "Valproic Acid", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valproic Acid", "active_ingredients": [{"name": "VALPROIC ACID", "strength": "250 mg/5mL"}], "application_number": "ANDA073178", "marketing_category": "ANDA", "marketing_start_date": "20240102", "listing_expiration_date": "20261231"}