# Ibuprofen and Pseudoephedrine hydrochloride

NDC: 51660-493
Generic name: ibuprofen and pseudoephedrine hydrochloride
Labeler / Manufacturer: Ohm Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, SUGAR COATED
Routes: ORAL
Marketing started: 20011013

FDA application: ANDA074567

## Active ingredients

- IBUPROFEN: 200 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-493"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-493
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb7fb0d3-adf6-4c14-ac61-103dc869ebf2