# Guaifenesin and Pseudoephedrine HCl

NDC: 51660-077
Generic name: Guaifenesin and Pseudoephedrine HCl
Labeler / Manufacturer: Ohm Laboratories, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210401

FDA application: ANDA212542

## Active ingredients

- GUAIFENESIN: 1200 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-077"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-077
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2521ecd3-28f3-a13c-e063-6394a90a7245