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Loratadine

NDC 68788-8605, Loratadine, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8605
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA211718
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8605 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LORATADINE10 mg/1
Package NDCNDC-11Package
68788-8605-06878886050010 TABLET in 1 BOTTLE (68788-8605-0)
68788-8605-16878886050114 TABLET in 1 BOTTLE (68788-8605-1)
68788-8605-36878886050330 TABLET in 1 BOTTLE (68788-8605-3)
68788-8605-56878886050515 TABLET in 1 BOTTLE (68788-8605-5)
68788-8605-96878886050990 TABLET in 1 BOTTLE (68788-8605-9)

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 68788-8605 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8605 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8605. 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.