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Guaifenesin and Dextromethorphan HBr

NDC 58602-871, Guaifenesin and Dextromethorphan HBr, tablet, extended release, from Aurohealth LLC.

Product NDC
58602-871
Status
Listed
Labeler
Aurohealth LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA206941
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/58602-871 \
  -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
58602-871-83586020871831 BLISTER PACK in 1 CARTON (58602-871-83) / 10 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 58602-871 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/58602-871 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.