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EXCAUGH

NDC 51467-009, Guaifenesin, tablet, from FORTUNE PHARMACAL COMPANY, LIMITED.

Product NDC
51467-009
Status
Listed
Labeler
FORTUNE PHARMACAL COMPANY, LIMITED
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M012
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51467-009 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GUAIFENESIN100 mg/1

Pharmacologic classes

Decreased Respiratory Secretion Viscosity [PE]; Expectorant [EPC]; Increased Respiratory Secretions [PE]

Package NDCNDC-11Package
51467-009-01514670009012 BLISTER PACK in 1 BOX (51467-009-01) / 12 TABLET in 1 BLISTER PACK
51467-009-02514670009023 BLISTER PACK in 1 BOX (51467-009-02) / 12 TABLET 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 51467-009 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51467-009 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51467-009. 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.