# Hydromorphone Hydrochloride

NDC: 13811-704
Generic name: Hydromorphone Hydrochloride
Labeler / Manufacturer: Trigen Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160915

FDA application: ANDA205629

## Active ingredients

- HYDROMORPHONE HYDROCHLORIDE: 32 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"13811-704"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13811-704
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8bb81796-6990-40e9-bee4-1f292f91ae99