United States · FDA National Drug Code directory

SAPROPTERIN DIHYDROCHLORIDE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
49884-873_d9caf600-36bf-443b-bd05-cfeef3d84522
Product NDC
49884-873
Form
POWDER, FOR SOLUTION
Composition / generic term
SAPROPTERIN DIHYDROCHLORIDE
Labeler
Par Health USA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20201001
Source listing expiry
20271231

Source-listed ingredients

  • SAPROPTERIN DIHYDROCHLORIDE — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 PACKET in 1 CARTON (49884-873-72) / 1 POWDER, FOR SOLUTION in 1 PACKET (49884-873-52) · 49884-873-72

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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