# Cimetidine

NDC: 0093-8192
Generic name: Cimetidine
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20031124

FDA application: ANDA074151

## Active ingredients

- CIMETIDINE: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-8192"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-8192
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=496e258d-a5fd-42da-9a86-73afc8be359b