Heparin Sodium

NDC 63739-920 · McKesson Corporation dba SKY Packaging

Generic nameHeparin Sodium

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS, SUBCUTANEOUS

Active ingredient(s)HEPARIN SODIUM

Strength1000 [USP'U]/mL

Pharmacologic classAnti-coagulant [EPC], Heparin [CS], Unfractionated Heparin [EPC]

Marketing categoryANDA

Packages

FDA lists these products with the same active ingredient.

63323-518 — HEPARIN SODIUM, 63323-519 — Heparin Sodium, 63323-522 — HEPARIN SODIUM, 63323-523 — HEPARIN SODIUM, 63323-540 — HEPARIN SODIUM, 63323-542 — HEPARIN SODIUM, 63323-543 — HEPARIN SODIUM, 63323-915 — HEPARIN SODIUM, 63739-900 — Heparin Sodium, 63739-901 — Heparin Sodium, 63739-931 — Heparin Sodium, 63739-942 — Heparin Sodium, 63739-953 — Heparin Sodium, 63739-964 — Heparin Sodium, 63739-975 — Heparin Sodium, 63739-986 — Heparin Sodium, 65219-066 — HEPARIN SODIUM, 67457-384 — Heparin Sodium, 68083-136 — Heparin Sodium, 68083-427 — Heparin Sodium, +102 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.