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Loratadine Allergy Relief

NDC 55289-728, Loratadine, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
55289-728
Status
Listed
Labeler
PD-Rx Pharmaceuticals, 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/55289-728 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LORATADINE10 mg/1
Package NDCNDC-11Package
55289-728-155528907281515 TABLET in 1 BOTTLE, PLASTIC (55289-728-15)
55289-728-205528907282020 TABLET in 1 BOTTLE, PLASTIC (55289-728-20)
55289-728-605528907286060 TABLET in 1 BOTTLE, PLASTIC (55289-728-60)
55289-728-905528907289090 TABLET in 1 BOTTLE, PLASTIC (55289-728-90)

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 55289-728 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55289-728 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55289-728. 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.