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Desloratadine

NDC 69339-194, Desloratadine, tablet, film coated, from Natco Pharma USA LLC.

Product NDC
69339-194
Status
Listed
Labeler
Natco Pharma USA LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078351
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69339-194 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DESLORATADINE5 mg/1

Pharmacologic classes

Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]

Package NDCNDC-11Package
69339-194-0169339019401100 TABLET, FILM COATED in 1 BOTTLE (69339-194-01)
69339-194-0569339019405500 TABLET, FILM COATED in 1 BOTTLE (69339-194-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e4db30a5-48e5-4fe3-8793-30b6866f87c1

  • NADAC price for package 69339019401

    GET /v1/drugs/nadac/69339019401

  • NADAC price for package 69339019405

    GET /v1/drugs/nadac/69339019405

Use it

Look up 69339-194 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69339-194 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69339-194. 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.