# Acetaminophen

NDC: 71335-9746
Generic name: Acetaminophen tablet extended release
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20211004

FDA application: ANDA215486

## 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:"71335-9746"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-9746
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=61ea1796-b9c7-4cb9-9a36-60943f884875
