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Loratadine antihistamine

NDC 72789-347, Loratadine, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-347
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA076301
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-347 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LORATADINE10 mg/1
Package NDCNDC-11Package
72789-347-147278903471414 TABLET in 1 BOTTLE, PLASTIC (72789-347-14)
72789-347-207278903472020 TABLET in 1 BOTTLE, PLASTIC (72789-347-20)
72789-347-307278903473030 TABLET in 1 BOTTLE, PLASTIC (72789-347-30)
72789-347-8772789034787300 TABLET in 1 BOTTLE, PLASTIC (72789-347-87)
72789-347-907278903479090 TABLET in 1 BOTTLE, PLASTIC (72789-347-90)

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 72789-347 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-347 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-347. 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.