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Desloratadine

NDC 69452-363, Desloratadine, tablet, film coated, from Bionpharma Inc..

Product NDC
69452-363
Status
Listed
Labeler
Bionpharma Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078357
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69452-363 \
  -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
69452-363-2069452036320100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-363-20)
69452-363-3069452036330500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-363-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4d094001-b85a-47b3-bc67-a46660384ece

  • NADAC price for package 69452036320

    GET /v1/drugs/nadac/69452036320

  • NADAC price for package 69452036330

    GET /v1/drugs/nadac/69452036330

Use it

Look up 69452-363 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69452-363 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69452-363. 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.