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Azithromycin Dihydrate

NDC 70518-4105, Azithromycin dihydrate, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4105
Status
Listed
Labeler
REMEDYREPACK INC.
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/70518-4105 \
  -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
70518-4105-07051841050030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4105-0)
70518-4105-1705184105015 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4105-1)
70518-4105-2705184105022 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4105-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7711e846-0bb3-486c-8511-f445e264cd98

Use it

Look up 70518-4105 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4105 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4105. 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.