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Mucus Relief

NDC 71610-499 · Aphena Pharma Solutions - Tennessee, LLC

Generic nameGuaifenesin
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)GUAIFENESIN
Strength600 mg/1
Marketing categoryANDA

Packages

71610-499-12 — 12 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-499-12)

71610-499-53 — 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-499-53)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2032 — Guaifenesin, 71335-2216 — Dextromethorphan Hydrobromide / Guaifenesin, 71335-2642 — Guaifenesin, 71335-9616 — Guaifenesin, 71399-0024 — Guaifenesin, 71399-0025 — Dextromethorphan HBr, Guaifenesin, 71399-0026 — Dextromethorphan HBr, Guaifenesin, 71399-0054 — Guaifenesin, 71610-098 — Guaifenesin 200 mg, 71610-434 — Guaifenesin, 71679-119 — Guaifenesin 400 mg, 71679-148 — Guaifenesin, 71679-309 — Guaifenesin, 71800-057 — DEXTROMETHORPHAN HYDROBROMIDE,GUAIFENESIN, 71800-059 — GUAIFENESIN, 72036-012 — Guaifenesin and Dextromethorphan HBr, 72036-119 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-155 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-167 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-175 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, +1437 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.