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NDC 21130-914, Loratadine, tablet, from Safeway, Inc..

Product NDC
21130-914
Status
Listed
Labeler
Safeway, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA075209
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/21130-914 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LORATADINE10 mg/1
Package NDCNDC-11Package
21130-914-102113009141010 BLISTER PACK in 1 CARTON (21130-914-10) / 1 TABLET in 1 BLISTER PACK
21130-914-12211300914121 BOTTLE, PLASTIC in 1 BOX (21130-914-12) / 120 TABLET in 1 BOTTLE, PLASTIC
21130-914-60211300914601 BOTTLE, PLASTIC in 1 BOX (21130-914-60) / 60 TABLET in 1 BOTTLE, PLASTIC

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 21130-914 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/21130-914 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 21130-914. 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.