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NDC 59212-702, prednisolone sodium phosphate, tablet, orally disintegrating, from Advanz Pharma (US) Corp..

Product NDC
59212-702
Status
Listed
Labeler
Advanz Pharma (US) Corp.
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA021959
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59212-702 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISOLONE SODIUM PHOSPHATE30 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
59212-702-12592120702122 BLISTER PACK in 1 CARTON (59212-702-12) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (59212-702-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1e379543-c4cf-4e72-953b-db15b7f0c2a1

Use it

Look up 59212-702 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59212-702 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59212-702. 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.