United States · FDA National Drug Code directory

Guaifenesin and Dextromethorphan Hydrobromide

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: 51316-600_4fe39452-8d46-ba50-e063-6294a90ac53a
Product NDC: 51316-600
Form: TABLET, EXTENDED RELEASE
Composition / generic term: Guaifenesin and Dextromethorphan Hydrobromide
Labeler: CVS PHARMACY, INC
Marketing category: ANDA
Marketing start / end (source format): 20220419
Source listing expiry: 20271231

Source-listed ingredients

GUAIFENESIN — 1200 mg/1
DEXTROMETHORPHAN HYDROBROMIDE — 60 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

5 BLISTER PACK in 1 CARTON (51316-600-70) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 51316-600-70

Source and coverage

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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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