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MUCUS RELIEF

NDC 71335-2032, Guaifenesin, tablet, from Bryant Ranch Prepack.

Product NDC
71335-2032
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-2032 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GUAIFENESIN400 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71335-2032-17133520320130 TABLET in 1 BOTTLE (71335-2032-1)
71335-2032-27133520320220 TABLET in 1 BOTTLE (71335-2032-2)
71335-2032-37133520320350 TABLET in 1 BOTTLE (71335-2032-3)
71335-2032-47133520320460 TABLET in 1 BOTTLE (71335-2032-4)
71335-2032-57133520320540 TABLET in 1 BOTTLE (71335-2032-5)

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 71335-2032 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2032 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2032. 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.