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Sodium Bicarbonate

NDC 0409-5555 · Hospira, Inc.

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameSODIUM BICARBONATE
Dosage formINJECTION, SOLUTION
RouteINTRAVENOUS
Active ingredient(s)SODIUM BICARBONATE
Strength42 mg/mL
Pharmacologic classAlkalinizing Activity [MoA]
Marketing categoryANDA

Packages

0409-5555-02 — 25 VIAL, SINGLE-USE in 1 TRAY (0409-5555-02) / 5 mL in 1 VIAL, SINGLE-USE (0409-5555-12)

0409-5555-01 — 25 VIAL, SINGLE-USE in 1 TRAY (0409-5555-01) / 5 mL in 1 VIAL, SINGLE-USE (0409-5555-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0280-4100 — Alka-Seltzer Gold, 0283-1023 — Laxative, 0363-0421 — Aspirin, Citric Acid, Sodium Bicarbonate, 0363-0541 — Aspirin, Citric Acid, Sodium Bicarbonate, 0363-0732 — Omeprazole, sodium bicarbonate, 0363-0801 — SODIUM BICARBONATE, SODIUM CHLORIDE, 0363-0802 — SODIUM BICARBONATE, SODIUM CHLORIDE, 0395-2685 — Sodium Bicarbonate, 0404-9951 — sodium bicarbonate, 0404-9980 — sodium bicarbonate, 0409-6625 — SODIUM BICARBONATE, 0409-6637 — Sodium Bicarbonate, 0536-1046 — Sodium Bicarbonate, 0536-1047 — Sodium Bicarbonate, 0615-8641 — Sodium Bicarbonate, 0802-2685 — Sodium Bicarbonate, 0904-7261 — Sodium Bicarbonate, 10095-100 — Sodium Bicarbonate, 10237-591 — Sodium Bicarbonate, 10361-793 — Antacid/AntiFlatulent, +214 more

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