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MUCUS RELIEF - DM MAXIMUM STRENGTH

NDC 73581-406, Guaifenesin, Dextromethorphan HBr, tablet, from YYBA CORP.

Product NDC
73581-406
Status
Listed
Labeler
YYBA CORP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA206941
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73581-406 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXTROMETHORPHAN HYDROBROMIDE60 mg/1
  • GUAIFENESIN1200 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
73581-406-01735810406012 BOTTLE in 1 CARTON (73581-406-01) / 50 TABLET in 1 BOTTLE (73581-406-05)
73581-406-057358104060550 TABLET in 1 BOTTLE (73581-406-05)

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 73581-406 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73581-406 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73581-406. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.