# Guaifenesin

NDC: 68001-561
Generic name: Guaifenesin
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230315

FDA application: ANDA210453

## Active ingredients

- GUAIFENESIN: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-561"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-561
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ee8a2a97-16aa-0f3e-e053-2a95a90a523b