# Arthritis Pain Relief

NDC: 68016-303
Generic name: Acetaminophen
Labeler / Manufacturer: CHAIN DRUG CONSORTIUM
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20200801
Marketing ended: 20260930
FDA application: ANDA211544

## Active ingredients

- ACETAMINOPHEN: 650 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68016-303"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68016-303
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=778a15d5-3fa4-4386-8afb-751f4537c10d