# acetaminophen pain reliever fever reducer

NDC: 45802-730
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: 20101028
Marketing ended: 20261130
FDA application: ANDA070608

## 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:"45802-730"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=45802-730
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b43974c3-4db9-4201-beee-b22596a2b241