United States · FDA National Drug Code directory

Enoxaparin 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
63323-584_2b6f0c59-240a-48ec-9cef-e55cc4b52274
Product NDC
63323-584
Form
INJECTION
Composition / generic term
Enoxaparin Sodium
Labeler
Fresenius Kabi USA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20190423
Source listing expiry
20271231

Source-listed ingredients

  • ENOXAPARIN SODIUM — 80 mg/.8mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 BLISTER PACK in 1 CARTON (63323-584-65) / 1 SYRINGE in 1 BLISTER PACK (63323-584-63) / .8 mL in 1 SYRINGE · 63323-584-65

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 →