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Loratadine

NDC 70010-162, Loratadine, tablet, from Granules Pharmaceuticals Inc..

Product NDC
70010-162
Status
Listed
Labeler
Granules Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA210722
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70010-162 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LORATADINE10 mg/1
Package NDCNDC-11Package
70010-162-0170010016201100 TABLET in 1 BOTTLE (70010-162-01)
70010-162-037001001620330 TABLET in 1 BOTTLE (70010-162-03)
70010-162-3470010016234300 TABLET in 1 BOTTLE (70010-162-34)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 70010016201

    GET /v1/drugs/nadac/70010016201

  • NADAC price for package 70010016234

    GET /v1/drugs/nadac/70010016234

Use it

Look up 70010-162 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70010-162 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70010-162. 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.