# berkley and jensen famotidine

NDC: 68391-300
Generic name: Famotidine
Labeler / Manufacturer: BJWC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20131209

FDA application: ANDA077351

## Active ingredients

- FAMOTIDINE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68391-300"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68391-300
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=93c857e4-72b3-433e-ae6f-281cd57e3996