# Guaifenesin Extended-Release

NDC: 68094-048
Generic name: Guaifenesin
Labeler / Manufacturer: Precision Dose Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, MULTILAYER, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230322

FDA application: ANDA078912

## 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:"68094-048"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68094-048
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=608b00c5-a2c7-4514-9b46-02954d6675d6