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Azithromycin Dihydrate

NDC 71205-430, Azithromycin Dihydrate, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-430
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208250
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-430 \
  -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
71205-430-04712050430044 TABLET, FILM COATED in 1 BOTTLE (71205-430-04)
71205-430-06712050430061 BLISTER PACK in 1 CARTON (71205-430-06) / 6 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8037c6f4-4881-4740-8229-2aee56141cd0

Use it

Look up 71205-430 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-430 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-430. 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.