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Zithromax

NDC 0069-4061, azithromycin dihydrate, tablet, film coated, from Pfizer Laboratories Div Pfizer Inc.

Product NDC
0069-4061
Status
Listed
Labeler
Pfizer Laboratories Div Pfizer Inc
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA050711
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0069-4061 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AZITHROMYCIN DIHYDRATE250 mg/1

Pharmacologic classes

Macrolide Antimicrobial [EPC]; Macrolides [CS]

Package NDCNDC-11Package
0069-4061-010006940610130 TABLET, FILM COATED in 1 BOTTLE (0069-4061-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/db52b91e-79f7-4cc1-9564-f2eee8e31c45

Use it

Look up 0069-4061 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0069-4061 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0069-4061. 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.