# Pseudoephedrine Hydrochloride

NDC: 37808-007
Generic name: Pseudoephedrine Hydrochloride
Labeler / Manufacturer: HEB
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190515

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:"37808-007"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-007
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d9b46ff2-8bde-47c0-bc63-b19dbe7e197b