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Loratadine

NDC 21130-526, Loratadine, tablet, from SAFEWAY INC..

Product NDC
21130-526
Status
Listed
Labeler
SAFEWAY 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/21130-526 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LORATADINE10 mg/1
Package NDCNDC-11Package
21130-526-13211300526131 BOTTLE in 1 CARTON (21130-526-13) / 120 TABLET in 1 BOTTLE
21130-526-31211300526313 BLISTER PACK in 1 CARTON (21130-526-31) / 10 TABLET in 1 BLISTER PACK
21130-526-38211300526381 BOTTLE in 1 CARTON (21130-526-38) / 365 TABLET in 1 BOTTLE
21130-526-43211300526431 BOTTLE in 1 CARTON (21130-526-43) / 45 TABLET in 1 BOTTLE
21130-526-69211300526691 BLISTER PACK in 1 CARTON (21130-526-69) / 10 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 21130-526 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/21130-526 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 21130-526. 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.