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NDC 85237-1650, Guaifenesin and Dextromethorphan Hydrobromide, tablet, extended release, from Select Consumer Group.

Product NDC
85237-1650
Status
Listed
Labeler
Select Consumer Group
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/85237-1650 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GUAIFENESIN600 mg/1
  • DEXTROMETHORPHAN HYDROBROMIDE30 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
85237-1650-1852371650012 TABLET, EXTENDED RELEASE in 1 POUCH (85237-1650-1)
85237-1650-38523716500320 POUCH in 1 CARTON (85237-1650-3) / 2 TABLET, EXTENDED RELEASE in 1 POUCH

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 85237-1650 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85237-1650 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85237-1650. 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.