# Feverall Childrens

NDC: 51672-2115
Generic name: Acetaminophen
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SUPPOSITORY
Routes: RECTAL
Marketing started: 20131212

FDA application: NDA018337

## Active ingredients

- ACETAMINOPHEN: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-2115"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-2115
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=861e2987-5473-45b0-b2a6-f980a9b0e809