# Arthritis Pain

NDC: 57344-200
Generic name: Acetaminophen
Labeler / Manufacturer: AAA Pharmaceutical, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250912

FDA application: ANDA211544

## Active ingredients

- ACETAMINOPHEN: 650 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57344-200"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57344-200
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e9b237c-5df4-9ec5-e063-6394a90a87de