# Morphine Sulfate Extended Release

NDC: 68084-158
Generic name: Morphine Sulfate
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20130926

FDA application: ANDA074862

## Active ingredients

- MORPHINE SULFATE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68084-158"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68084-158
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f915420d-981d-455b-b4cf-67c8e201a136