United States · FDA National Drug Code directory

Heparin Sodium

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
63323-542_e59b46ab-12ac-4ae9-bd13-3146984037e0
Product NDC
63323-542
Form
INJECTION, SOLUTION
Composition / generic term
HEPARIN SODIUM
Labeler
Fresenius Kabi USA, LLC
Marketing category
NDA
Marketing start / end (source format)
20191104
Source listing expiry
20271231

Source-listed ingredients

  • HEPARIN SODIUM — 10000 [USP'U]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 25 VIAL in 1 TRAY (63323-542-13) / 1 mL in 1 VIAL (63323-542-09) · 63323-542-13
  • 25 VIAL in 1 TRAY (63323-542-14) / 5 mL in 1 VIAL (63323-542-04) · 63323-542-14

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →