# acetaminophen for children

NDC: 45802-732
Generic name: Acetaminophen
Labeler / Manufacturer: Padagis Israel Pharmaceuticals Ltd
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUPPOSITORY
Routes: RECTAL
Marketing started: 20101214
Marketing ended: 20260930
FDA application: ANDA070607

## 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:"45802-732"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=45802-732
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=62b3d354-d7f5-4ba0-b233-ea6be0d7ff03