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Heparin Sodium

NDC 0781-3541 · Sandoz Inc.

Generic nameHeparin Sodium
Dosage formINJECTION, SOLUTION
RouteINTRAVENOUS, SUBCUTANEOUS
Active ingredient(s)HEPARIN SODIUM
Strength20000 [USP'U]/mL
Pharmacologic classAnti-coagulant [EPC], Heparin [CS], Unfractionated Heparin [EPC]
Marketing categoryANDA

Packages

0781-3541-25 — 25 VIAL, MULTI-DOSE in 1 CARTON (0781-3541-25) / 1 mL in 1 VIAL, MULTI-DOSE (0781-3541-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0409-7650 — HEPARIN SODIUM, 0641-0391 — Heparin Sodium, 0641-0400 — Heparin Sodium, 0641-0410 — Heparin Sodium, 0641-6199 — Heparin sodium, 0641-6204 — Heparin Sodium, 0781-3439 — Heparin Sodium, 0781-3533 — Heparin Sodium, 0781-3538 — Heparin Sodium, 0781-3540 — Heparin Sodium, 0781-3543 — Heparin Sodium, 0781-3545 — Heparin Sodium, 0781-3550 — Heparin Sodium, 0781-3555 — Heparin Sodium, 25021-400 — Heparin Sodium, 25021-401 — heparin sodium, 25021-402 — Heparin Sodium, 25021-403 — Heparin Sodium, 25021-404 — heparin sodium, 51662-1409 — HEPARIN SODIUM, +102 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.