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GUAIFENESIN

NDC 62207-840, GUAIFENESIN, tablet, extended release, from Granules India Ltd.

Product NDC
62207-840
Status
Listed
Labeler
Granules India Ltd
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/62207-840 \
  -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
62207-840-71622070840717 BLISTER PACK in 1 CARTON (62207-840-71) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
62207-840-936220708409310000 TABLET, EXTENDED RELEASE in 1 BOX (62207-840-93)
62207-840-99622070840994200 TABLET, EXTENDED RELEASE in 1 BAG (62207-840-99)

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 62207-840 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62207-840 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62207-840. 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.