# Valproic Acid

NDC: 17856-0152
Generic name: Valproic Acid
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20160715

FDA application: ANDA073484

## Active ingredients

- VALPROIC ACID: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17856-0152"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0152
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=453444b6-1f50-49de-ab3c-1e429c83bffa