valproic acid

Generic: valproic acid

Labeler: kesin pharma corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valproic acid
Generic Name valproic acid
Labeler kesin pharma corporation
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

valproic acid 250 mg/5mL

Manufacturer
Kesin Pharma Corporation

Identifiers & Regulatory

Product NDC 81033-266
Product ID 81033-266_3a214bf4-ea91-0892-e063-6394a90a9a9d
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 81033266
Hyphenated Format 81033-266

Supplemental Identifiers

RxCUI
1099687
UNII
614OI1Z5WI
NUI
N0000175753 N0000008486 N0000175751

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
  • 100 CUP, UNIT-DOSE in 1 CASE (81033-266-50) / 5 mL in 1 CUP, UNIT-DOSE (81033-266-05)
  • 100 CUP, UNIT-DOSE in 1 CASE (81033-266-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-266-10)
source: ndc

Packages (2)

81033-266-50 100 CUP, UNIT-DOSE in 1 CASE (81033-266-50) / 5 mL in 1 CUP, UNIT-DOSE (81033-266-05) 81033-266-52 100 CUP, UNIT-DOSE in 1 CASE (81033-266-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-266-10)

Ingredients (1)

valproic acid (250 mg/5mL)

Linked Drug Pages (1)

Valproic Acid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a214bf4-ea91-0892-e063-6394a90a9a9d", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751"], "unii": ["614OI1Z5WI"], "rxcui": ["1099687"], "spl_set_id": ["3a2155d0-e79d-3e11-e063-6294a90a4aae"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]", "Mood Stabilizer [EPC]"], "manufacturer_name": ["Kesin Pharma Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-266-50)  / 5 mL in 1 CUP, UNIT-DOSE (81033-266-05)", "package_ndc": "81033-266-50", "marketing_start_date": "20250801"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-266-52)  / 10 mL in 1 CUP, UNIT-DOSE (81033-266-10)", "package_ndc": "81033-266-52", "marketing_start_date": "20250801"}], "brand_name": "Valproic Acid", "product_id": "81033-266_3a214bf4-ea91-0892-e063-6394a90a9a9d", "dosage_form": "SOLUTION", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "81033-266", "generic_name": "Valproic Acid", "labeler_name": "Kesin Pharma Corporation", "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"}