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PREDNISOLONE ACETATE

NDC 68071-2222, prednisolone acetate, suspension/ drops, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-2222
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
SUSPENSION/ DROPS
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA017011
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2222 \
  -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
68071-2222-5680712222051 BOTTLE, DROPPER in 1 CARTON (68071-2222-5) / 5 mL in 1 BOTTLE, DROPPER

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ab72cf3d-7660-41b1-e053-2995a90a7f44

Use it

Look up 68071-2222 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2222 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-2222. 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.