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PRED FORTE

NDC 11980-180, prednisolone acetate, suspension/ drops, from Allergan, Inc..

Product NDC
11980-180
Status
Listed
Labeler
Allergan, Inc.
Dosage form
SUSPENSION/ DROPS
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA017011
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/11980-180 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISOLONE ACETATE10 mg/mL

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

Package NDCNDC-11Package
11980-180-05119800180051 BOTTLE, DROPPER in 1 CARTON (11980-180-05) / 5 mL in 1 BOTTLE, DROPPER

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/00a5aa88-e361-4ea7-8922-530c738b726e

  • NADAC price for package 11980018005

    GET /v1/drugs/nadac/11980018005

Use it

Look up 11980-180 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/11980-180 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 11980-180. 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.