# Ibuprofen and Pseudoephedrine hydrochloride

NDC: 51660-423
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

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-423"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-423
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=65ec0f85-7ca3-4adc-b152-a0ae2fd0692f