# Primidone

NDC: 0527-1301
Generic name: Primidone
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20010524

FDA application: ANDA084903

## Active ingredients

- PRIMIDONE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0527-1301"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0527-1301
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a1a817f7-c190-4825-94eb-442f477187e3