# Acetaminophen

NDC: 53329-643
Generic name: Acetaminophen
Labeler / Manufacturer: Medline Industries, LP
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20020430
Marketing ended: 20261231
FDA application: ANDA076200

## 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:"53329-643"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53329-643
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9f18d455-55ce-482c-8da8-dcb664038c6c