# Acetaminophen

NDC: 0904-7314
Generic name: Acetaminophen
Labeler / Manufacturer: MAJOR PHARMACEUTICALS
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230303

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:"0904-7314"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7314
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=efd0a432-abbb-1f88-e053-2995a90a8ce5