valproic acid

Generic: valproic acid

Labeler: atlantic biologicals corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valproic acid
Generic Name valproic acid
Labeler atlantic biologicals corp.
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

valproic acid 250 mg/1

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-0152
Product ID 17856-0152_38930d1f-1f70-1fa5-e063-6394a90a5c21
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073484
Listing Expiration 2026-12-31
Marketing Start 2016-07-15

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 178560152
Hyphenated Format 17856-0152

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 ANDA073484 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 POUCH in 1 BOX, UNIT-DOSE (17856-0152-1) / 1 CAPSULE, LIQUID FILLED in 1 POUCH
source: ndc

Packages (1)

17856-0152-1 100 POUCH in 1 BOX, UNIT-DOSE (17856-0152-1) / 1 CAPSULE, LIQUID FILLED in 1 POUCH

Ingredients (1)

valproic acid (250 mg/1)

Linked Drug Pages (1)

Valproic Acid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "38930d1f-1f70-1fa5-e063-6394a90a5c21", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751"], "unii": ["614OI1Z5WI"], "rxcui": ["1099681"], "spl_set_id": ["453444b6-1f50-49de-ab3c-1e429c83bffa"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]", "Mood Stabilizer [EPC]"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX, UNIT-DOSE (17856-0152-1)  / 1 CAPSULE, LIQUID FILLED in 1 POUCH", "package_ndc": "17856-0152-1", "marketing_start_date": "20210625"}], "brand_name": "Valproic Acid", "product_id": "17856-0152_38930d1f-1f70-1fa5-e063-6394a90a5c21", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "17856-0152", "generic_name": "Valproic Acid", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valproic Acid", "active_ingredients": [{"name": "VALPROIC ACID", "strength": "250 mg/1"}], "application_number": "ANDA073484", "marketing_category": "ANDA", "marketing_start_date": "20160715", "listing_expiration_date": "20261231"}