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Bosentan

NDC 47335-038, Bosentan, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-038
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209324
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-038 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BOSENTAN62.5 mg/1

Pharmacologic classes

Cytochrome P450 2C9 Inducers [MoA]; Cytochrome P450 3A Inducers [MoA]; Endothelin Receptor Antagonist [EPC]; Endothelin Receptor Antagonists [MoA]

Package NDCNDC-11Package
47335-038-644733500386410 BLISTER PACK in 1 CARTON (47335-038-64) / 3 TABLET, FILM COATED in 1 BLISTER PACK (47335-038-60)
47335-038-864733500388660 TABLET, FILM COATED in 1 BOTTLE (47335-038-86)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c006d8ef-8cb7-4fb3-88eb-b2debc302a20

Use it

Look up 47335-038 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-038 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-038. 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.