United States · FDA National Drug Code directory

Mucus Relief DM

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
37808-733_d2aca5b5-2bb6-41b5-a614-f470d233c98e
Product NDC
37808-733
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Guaifenesin, Dextromethorphan HBr
Labeler
H E B
Marketing category
ANDA
Marketing start / end (source format)
20230228
Source listing expiry
20261231

Source-listed ingredients

  • GUAIFENESIN — 600 mg/1
  • DEXTROMETHORPHAN HYDROBROMIDE — 30 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, PLASTIC in 1 BOX (37808-733-20) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC · 37808-733-20
  • 1 BOTTLE, PLASTIC in 1 BOX (37808-733-40) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC · 37808-733-40

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Mucus Relief DM — United States | Molindra Medicines