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Azithromycin Dihydrate

NDC 83112-501, Azithromycin Dihydrate, tablet, film coated, from Health Department, Oklahoma State.

Product NDC
83112-501
Status
Listed
Labeler
Health Department, Oklahoma State
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/83112-501 \
  -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
83112-501-00831120501002 TABLET, FILM COATED in 1 PACKET (83112-501-00)
83112-501-02831120501022 TABLET, FILM COATED in 1 PACKET (83112-501-02)
83112-501-04831120501044 TABLET, FILM COATED in 1 PACKET (83112-501-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4747c5d8-4831-c725-e063-6394a90a4fda

Use it

Look up 83112-501 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/83112-501 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 83112-501. 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.