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Guaifenesin and Dextromethorphan HBr

NDC 63304-106, Guaifenesin and Dextromethorphan HBr, tablet, extended release, from SUN PHARMACEUTICAL INDUSTRIES, INC..

Product NDC
63304-106
Status
Listed
Labeler
SUN PHARMACEUTICAL INDUSTRIES, INC.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA214781
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63304-106 \
  -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
63304-106-21633040106211 BLISTER PACK in 1 CARTON (63304-106-21) / 20 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 63304-106 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-106 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-106. 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.