# Pseudoephedrine hydrochloride

NDC: 51660-204
Generic name: Pseudoephedrine hydrochloride
Labeler / Manufacturer: Ohm Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20060428

FDA application: ANDA077442

## Active ingredients

- PSEUDOEPHEDRINE HYDROCHLORIDE: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-204"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-204
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4e98dd9f-4ab9-4d95-95b0-799ce217da70