# Acetaminophen

NDC: 63868-660
Generic name: Acetaminophen
Labeler / Manufacturer: CHAIN DRUG MARKETING ASSOCIATION INC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20200801
Marketing ended: 20261231
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:"63868-660"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63868-660
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2e30754a-42f7-4da2-944c-be61cee47b43