# Pain Relief 8 HR

NDC: 37808-747
Generic name: Acetaminophen
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170224

FDA application: ANDA075077

## Active ingredients

- ACETAMINOPHEN: 650 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-747"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-747
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b5c7e93b-e626-49c3-a7d4-773475f945ae