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Mucinex DM Maximum Strength

NDC 63824-072, Guaifenesin and Dextromethorphan Hydrobromide, tablet, extended release, from Reckitt Benckiser LLC.

Product NDC
63824-072
Status
Listed
Labeler
Reckitt Benckiser LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
NDA
Application
NDA021620
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63824-072 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GUAIFENESIN1200 mg/1
  • DEXTROMETHORPHAN HYDROBROMIDE60 mg/1

Pharmacologic classes

Decreased Respiratory Secretion Viscosity [PE]; Expectorant [EPC]; Increased Respiratory Secretions [PE]; Sigma-1 Agonist [EPC]; Sigma-1 Receptor Agonists [MoA]; Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]; Uncompetitive NMDA Receptor Antagonists [MoA]

Package NDCNDC-11Package
63824-072-02638240072021 POUCH in 1 CARTON (63824-072-02) / 1 TABLET, EXTENDED RELEASE in 1 POUCH
63824-072-07638240072071 BLISTER PACK in 1 CARTON (63824-072-07) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-072-35638240072351 BLISTER PACK in 1 CARTON (63824-072-35) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-072-36638240072362 BLISTER PACK in 1 CARTON (63824-072-36) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-072-46638240072463 BLISTER PACK in 1 CARTON (63824-072-46) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-072-48638240072484 BLISTER PACK in 1 CARTON (63824-072-48) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63824-072-56638240072564 BLISTER PACK in 1 CARTON (63824-072-56) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 63824-072 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63824-072 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63824-072. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.