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Guaifenesin 600 mg

NDC 25000-042, Guaifenesin 600 mg, tablet, from MARKSANS PHARMA LIMITED.

Product NDC
25000-042
Status
Listed
Labeler
MARKSANS PHARMA LIMITED
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA217780
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25000-042 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GUAIFENESIN600 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
25000-042-01250000042011 BOTTLE in 1 CARTON (25000-042-01) / 20 TABLET in 1 BOTTLE
25000-042-1225000004212500 TABLET in 1 BOTTLE (25000-042-12)
25000-042-55250000042552 BLISTER PACK in 1 CARTON (25000-042-55) / 10 TABLET in 1 BLISTER PACK
25000-042-99250000042992 BLISTER PACK in 1 CARTON (25000-042-99) / 20 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 25000-042 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25000-042 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25000-042. 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.