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Loratadine

NDC 68788-4103, Loratadine, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4103
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA208314
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4103 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LORATADINE10 mg/1
Package NDCNDC-11Package
68788-4103-06878841030010 TABLET in 1 BOTTLE (68788-4103-0)
68788-4103-16878841030114 TABLET in 1 BOTTLE (68788-4103-1)
68788-4103-36878841030330 TABLET in 1 BOTTLE (68788-4103-3)
68788-4103-56878841030515 TABLET in 1 BOTTLE (68788-4103-5)
68788-4103-96878841030990 TABLET in 1 BOTTLE (68788-4103-9)

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 68788-4103 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4103 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4103. 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.