# GUAIFENESIN

NDC: 62207-840
Generic name: GUAIFENESIN
Labeler / Manufacturer: Granules India Ltd
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20201218

FDA application: ANDA213420

## Active ingredients

- GUAIFENESIN: 1200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62207-840"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62207-840
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e3531e9e-2ae7-4188-b95a-90f35613fc05