valproic acid
Generic: valproic acid
Labeler: ani pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
valproic acid
Generic Name
valproic acid
Labeler
ani pharmaceuticals, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
valproic acid 250 mg/5mL
Manufacturer
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62559266
Hyphenated Format
62559-266
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 250 mg/5mL
Packaging
- 473 mL in 1 BOTTLE (62559-266-16)
Packages (1)
Ingredients (1)
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"}