United States · FDA National Drug Code directory
SODIUM BICARBONATE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 81298-7620_1a255946-a137-4e13-8203-65dd80b34872
- Product NDC
- 81298-7620
- Form
- SOLUTION
- Composition / generic term
- sodium bicarbonate injection,
- Labeler
- Long Grove Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240930
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM BICARBONATE — 84 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 20 VIAL in 1 CARTON (81298-7620-3) / 50 mL in 1 VIAL (81298-7620-1) · 81298-7620-3
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →