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Mucus Relief Extended Release Maximum Strength

NDC 37808-762, Guaifenesin, tablet, from H E B.

Product NDC
37808-762
Status
Listed
Labeler
H E B
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA207342
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/37808-762 \
  -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
37808-762-14378080762141 BOTTLE, PLASTIC in 1 BOX (37808-762-14) / 14 TABLET in 1 BOTTLE, PLASTIC
37808-762-42378080762421 BOTTLE, PLASTIC in 1 BOX (37808-762-42) / 42 TABLET in 1 BOTTLE, PLASTIC

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 37808-762 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/37808-762 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 37808-762. 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.