valproic acid

Generic: valproic acid

Labeler: chartwell governmental & specialty rx, llc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valproic acid
Generic Name valproic acid
Labeler chartwell governmental & specialty rx, llc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

valproic acid 250 mg/5mL

Manufacturer
Chartwell Governmental & Specialty RX, LLC.

Identifiers & Regulatory

Product NDC 68999-196
Product ID 68999-196_43f6119e-621e-ca3f-e063-6394a90a562e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075782
Listing Expiration 2026-12-31
Marketing Start 2000-12-22

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 68999196
Hyphenated Format 68999-196

Supplemental Identifiers

RxCUI
1099687
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 ANDA075782 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 2 TRAY in 1 BOX (68999-196-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-196-45)
source: ndc

Packages (1)

68999-196-24 2 TRAY in 1 BOX (68999-196-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-196-45)

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": "43f6119e-621e-ca3f-e063-6394a90a562e", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751"], "unii": ["614OI1Z5WI"], "rxcui": ["1099687"], "spl_set_id": ["5d19f389-7180-4e01-845f-519b7ea60ba0"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]", "Mood Stabilizer [EPC]"], "manufacturer_name": ["Chartwell Governmental & Specialty RX, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (68999-196-24)  / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-196-45)", "package_ndc": "68999-196-24", "marketing_start_date": "20251114"}], "brand_name": "Valproic Acid", "product_id": "68999-196_43f6119e-621e-ca3f-e063-6394a90a562e", "dosage_form": "SOLUTION", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "68999-196", "generic_name": "Valproic Acid", "labeler_name": "Chartwell Governmental & Specialty RX, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valproic Acid", "active_ingredients": [{"name": "VALPROIC ACID", "strength": "250 mg/5mL"}], "application_number": "ANDA075782", "marketing_category": "ANDA", "marketing_start_date": "20001222", "listing_expiration_date": "20261231"}