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Sapropterin Dihydrochloride

NDC 52817-850, Sapropterin Dihydrochloride, powder, for solution, from TRUPHARMA, LLC.

Product NDC
52817-850
Status
Listed
Labeler
TRUPHARMA, LLC
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216432
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/52817-850 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SAPROPTERIN DIHYDROCHLORIDE100 mg/1

Pharmacologic classes

Breast Cancer Resistance Protein Inhibitors [MoA]; P-Glycoprotein Inhibitors [MoA]; Phenylalanine Hydroxylase Activator [EPC]; Phenylalanine Hydroxylase Activators [MoA]

Package NDCNDC-11Package
52817-850-01528170850011 POWDER, FOR SOLUTION in 1 POUCH (52817-850-01)
52817-850-305281708503030 POWDER, FOR SOLUTION in 1 CARTON (52817-850-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/39f1d020-4359-401b-88a8-ed25eaa40b45

Use it

Look up 52817-850 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/52817-850 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 52817-850. 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.