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Pretomanid

NDC 49502-476, Pretomanid, tablet, from Viatris Specialty LLC.

Product NDC
49502-476
Status
Listed
Labeler
Viatris Specialty LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA212862
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49502-476 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRETOMANID200 mg/1

Pharmacologic classes

Antimycobacterial [EPC]; Organic Anion Transporter 3 Inhibitors [MoA]

Package NDCNDC-11Package
49502-476-26495020476261 BOTTLE in 1 CARTON (49502-476-26) / 26 TABLET in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f1906fc9-cb3c-4e13-8a4a-da76100c1bf3

Use it

Look up 49502-476 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49502-476 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49502-476. 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.