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Azithromycin Dihydrate

NDC 71205-491, Azithromycin Dihydrate, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-491
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208249
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-491 \
  -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
71205-491-03712050491033 TABLET, FILM COATED in 1 BLISTER PACK (71205-491-03)
71205-491-04712050491044 TABLET, FILM COATED in 1 BLISTER PACK (71205-491-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bb97a057-2537-41ae-b50c-a80605039c30

Use it

Look up 71205-491 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-491 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-491. 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.