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Azithromycin

NDC 50111-789, Azithromycin, tablet, film coated, from Teva Pharmaceuticals USA, Inc..

Product NDC
50111-789
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA065218
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50111-789 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AZITHROMYCIN MONOHYDRATE600 mg/1

Pharmacologic classes

Macrolide Antimicrobial [EPC]; Macrolides [CS]

Package NDCNDC-11Package
50111-789-105011107891030 TABLET, FILM COATED in 1 BOTTLE (50111-789-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ac549022-4d7f-4c9f-9244-1a2df9a27276

  • NADAC price for package 50111078910

    GET /v1/drugs/nadac/50111078910

Use it

Look up 50111-789 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50111-789 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50111-789. 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.