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Loratadine

NDC 63868-151, Loratadine, tablet, from Chain Drug Marketing Association Inc..

Product NDC
63868-151
Status
Listed
Labeler
Chain Drug Marketing Association Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA076134
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63868-151 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LORATADINE10 mg/1
Package NDCNDC-11Package
63868-151-0163868015101100 TABLET in 1 BOTTLE (63868-151-01)
63868-151-106386801511010 TABLET in 1 BLISTER PACK (63868-151-10)
63868-151-306386801513030 TABLET in 1 BLISTER PACK (63868-151-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 63868-151 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63868-151 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63868-151. 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.