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Mucus Relief

NDC 72090-012, Guaifenesin, tablet, extended release, from Pioneer Life Sciences, LLC.

Product NDC
72090-012
Status
Listed
Labeler
Pioneer Life Sciences, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA213420
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72090-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GUAIFENESIN1200 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72090-012-0172090001201100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-01)
72090-012-027209000120230 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-02)
72090-012-037209000120350 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-03)

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 72090-012 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72090-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72090-012. 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.