valproic acid

Generic: valproic acid

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valproic acid
Generic Name valproic acid
Labeler direct_rx
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

valproic acid 250 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-010
Product ID 72189-010_2c290b36-b0f4-2265-e063-6394a90af311
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073229
Listing Expiration 2026-12-31
Marketing Start 2019-06-21

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 72189010
Hyphenated Format 72189-010

Supplemental Identifiers

RxCUI
1099681
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 ANDA073229 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (72189-010-30)
source: ndc

Packages (1)

Ingredients (1)

valproic acid (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c290b36-b0f4-2265-e063-6394a90af311", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751"], "unii": ["614OI1Z5WI"], "rxcui": ["1099681"], "spl_set_id": ["8bdbacb1-b38a-3282-e053-2a95a90af022"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]", "Mood Stabilizer [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-010-30)", "package_ndc": "72189-010-30", "marketing_start_date": "20190621"}], "brand_name": "Valproic Acid", "product_id": "72189-010_2c290b36-b0f4-2265-e063-6394a90af311", "dosage_form": "CAPSULE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "72189-010", "generic_name": "Valproic Acid", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valproic Acid", "active_ingredients": [{"name": "VALPROIC ACID", "strength": "250 mg/1"}], "application_number": "ANDA073229", "marketing_category": "ANDA", "marketing_start_date": "20190621", "listing_expiration_date": "20261231"}