# CIMETIDINE

NDC: 62135-633
Generic name: CIMETIDINE
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19940517

FDA application: ANDA074329

## Active ingredients

- CIMETIDINE: 800 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62135-633"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-633
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=01997826-7ca1-473e-bfc9-075b14b58a35