# Ramelteon

NDC: 43598-741
Generic name: Ramelteon
Labeler / Manufacturer: Dr.Reddys Laboratories Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190722
Marketing ended: 20260731
FDA application: ANDA091693

## Active ingredients

- RAMELTEON: 8 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-741"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-741
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b71cd925-1bae-5a6a-072b-941ad6d3ce65