# Pseudoephedrine Hydrochloride

NDC: 63868-143
Generic name: Pseudoephedrine Hydrochloride
Labeler / Manufacturer: Chain Drug Marketing Association Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
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:"63868-143"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63868-143
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=880d368f-0ce3-4993-b5b1-13bf01310516