# GUAIFENESIN

NDC: 62207-570
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: 20210201

FDA application: ANDA213420

## 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:"62207-570"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62207-570
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ba7c1e26-b7d0-4aea-e053-2a95a90a903e