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Loratadine Allergy Relief

NDC 37808-529, Loratadine, tablet, from HEB.

Product NDC
37808-529
Status
Listed
Labeler
HEB
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/37808-529 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LORATADINE10 mg/1
Package NDCNDC-11Package
37808-529-0137808052901100 TABLET in 1 BOTTLE (37808-529-01)
37808-529-11378080529111 BLISTER PACK in 1 CARTON (37808-529-11) / 10 TABLET in 1 BLISTER PACK
37808-529-313780805293130 BLISTER PACK in 1 CARTON (37808-529-31) / 1 TABLET in 1 BLISTER PACK

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 37808-529 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/37808-529 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 37808-529. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.