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Robitussin 12 Hour Cough Relief

NDC 0031-8655, dextromethorphan polistirex, suspension, extended release, from Haleon US Holdings LLC.

Product NDC
0031-8655
Status
Listed
Labeler
Haleon US Holdings LLC
Dosage form
SUSPENSION, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA091135
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0031-8655 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXTROMETHORPHAN HYDROBROMIDE30 mg/5mL

Pharmacologic classes

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
0031-8655-10000318655101 BOTTLE in 1 CARTON (0031-8655-10) / 89 mL in 1 BOTTLE

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 0031-8655 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0031-8655 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0031-8655. 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.