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NDC 36800-611, loratadine, pseudoephedrine sulfate, tablet, film coated, extended release, from Topco Associates LLC.

Product NDC
36800-611
Status
Listed
Labeler
Topco Associates LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA076050
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/36800-611 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LORATADINE5 mg/1
  • PSEUDOEPHEDRINE SULFATE120 mg/1

Pharmacologic classes

Adrenergic alpha-Agonists [MoA]; alpha-Adrenergic Agonist [EPC]

Package NDCNDC-11Package
36800-611-653680006116530 BLISTER PACK in 1 CARTON (36800-611-65) / 1 TABLET, FILM COATED, EXTENDED RELEASE 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 36800-611 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/36800-611 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 36800-611. 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.