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NDC 56062-555, loratadine, Pseudoephedrine sulfate, tablet, film coated, extended release, from Publix Super Markets Inc.

Product NDC
56062-555
Status
Listed
Labeler
Publix Super Markets Inc
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/56062-555 \
  -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
56062-555-465606205554610 BLISTER PACK in 1 CARTON (56062-555-46) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
56062-555-605606205556020 BLISTER PACK in 1 CARTON (56062-555-60) / 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 56062-555 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/56062-555 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 56062-555. 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.