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azithromycin dihydrate

NDC 70436-220, azithromycin dihydrate, powder, for suspension, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-220
Status
Listed
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217036
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-220 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AZITHROMYCIN DIHYDRATE100 mg/5mL

Pharmacologic classes

Macrolide Antimicrobial [EPC]; Macrolides [CS]

Package NDCNDC-11Package
70436-220-34704360220341 BOTTLE in 1 CARTON (70436-220-34) / 15 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/33d4ac05-b564-440c-971d-b78590dd2c32

Use it

Look up 70436-220 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-220 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-220. 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.