# Maximum Strength Mucus Relief

NDC: 63868-148
Generic name: Guaifenesin
Labeler / Manufacturer: CHAIN DRUG MARKETING ASSOCIATION INC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210917
Marketing ended: 20270228
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:"63868-148"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63868-148
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c20f64e3-485b-4ea7-b73d-56e5c898ed2e