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Sodium Bicarbonate

NDC 81665-200 · OMNIVIUM PHARMACEUTICALS LLC.

Generic nameSODIUM BICARBONATE

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS

Active ingredient(s)SODIUM BICARBONATE

Strength84 mg/mL

Pharmacologic classAlkalinizing Activity [MoA]

Marketing categoryANDA

Packages

81665-200-05 — 20 VIAL in 1 CARTON (81665-200-05) / 50 mL in 1 VIAL (81665-200-01)

81665-200-25 — 25 VIAL in 1 CARTON (81665-200-25) / 50 mL in 1 VIAL (81665-200-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76328-223 — SODIUM BICARBONATE, 76329-3352 — Sodium Bicarbonate, 77333-829 — Sodium Bicarbonate, 78271-041 — Sodium Bicarbonate, 79481-0502 — SODIUM BICARBONATE, SODIUM CHLORIDE, 79903-013 — Omeprazole, sodium bicarbonate, 80513-611 — Sodium Bicarbonate, 80830-2305 — sodium bicarbonate, 80830-2613 — Sodium Bicarbonate, 81298-7620 — sodium bicarbonate injection,, 81943-502 — Hemodialysis Grade Sodium Bicarbonate Solution, 81943-503 — Hemodialysis Grade Sodium Bicarbonate Solution, 82449-000 — SODIUM BICARBONATE, 82632-100 — Omeprazole, Sodium Bicarbonate, 82632-699 — omepraole, sodium bicarbonate, 82645-904 — Sodium Bicarbonate, 82876-501 — Allantoin, 82876-502 — Allantoin, 82876-503 — Allantoin, 82876-504 — Allantoin, +214 more

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