# Carbamazepine

NDC: 0093-0109
Generic name: Carbamazepine
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19900930
Marketing ended: 20260731
FDA application: ANDA070541

## Active ingredients

- CARBAMAZEPINE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-0109"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-0109
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bfd63965-56e6-4af7-b7ef-45a5105d4d35