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Sodium Bicarbonate

NDC 51754-5012 · Exela Pharma Sciences, LLC

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

Packages

51754-5012-4 — 25 VIAL in 1 CARTON (51754-5012-4) / 10 mL in 1 VIAL

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51662-1310 — INFANT 4.2% SODIUM BICARBONATE, 51662-1383 — SODIUM BICARBONATE, 51662-1400 — SODIUM BICARBONATE, 51662-1463 — 7.5% SODIUM BICARBONATE, 51662-1472 — PEDIATRIC 8.4% SODIUM BICARBONATE, 51662-1497 — SODIUM BICARBONATE, 51662-1573 — SODIUM BICARBONATE, 51754-5001 — SODIUM BICARBONATE, 51754-5002 — SODIUM BICARBONATE, 51754-5011 — SODIUM BICARBONATE, 51754-8888 — SODIUM BICARBONATE, 52268-100 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 52536-236 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 52536-302 — polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloride, 53041-663 — Omeprazole, Sodium bicarbonate, 53041-664 — Omeprazole, Sodium bicarbonate, 53145-300 — Sodium Bicarbonate, 53145-390 — Sodium Bicarbonate, 53942-421 — Aspirin, Citric Acid, Sodium Bicarbonate, 53943-421 — Aspirin, Citric Acid, Sodium Bicarbonate, +214 more

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