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
- 81952-115_2e8e07a4-763e-79e5-e063-6394a90a7619
- Product NDC
- 81952-115
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Heparin Sodium
- Labeler
- Hepalink USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140612
- Source listing expiry
- 20261231
Source-listed ingredients
- HEPARIN SODIUM — 1000 [USP'U]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, SINGLE-DOSE in 1 CARTON (81952-115-07) / 2 mL in 1 VIAL, SINGLE-DOSE (81952-115-02) · 81952-115-07
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 →