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Azithromycin

NDC 71205-519, Azithromycin, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-519
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207398
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-519 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AZITHROMYCIN DIHYDRATE500 mg/1

Pharmacologic classes

Macrolide Antimicrobial [EPC]; Macrolides [CS]

Package NDCNDC-11Package
71205-519-03712050519031 BLISTER PACK in 1 CARTON (71205-519-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK
71205-519-307120505193030 TABLET, FILM COATED in 1 BOTTLE (71205-519-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/25f2d819-ae38-4061-a897-bbcfce3739bf

Use it

Look up 71205-519 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-519 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-519. 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.