# Acetaminophen

NDC: 79903-132
Generic name: Acetaminophen
Labeler / Manufacturer: WALMART INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220726

FDA application: ANDA207229

## Active ingredients

- ACETAMINOPHEN: 650 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"79903-132"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=79903-132
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0035a4fd-8dd5-4534-a1b5-f510d637f721