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
- 83854-001_38887da2-9f53-8db2-e063-6294a90a7738
- Product NDC
- 83854-001
- Form
- INJECTION, SOLUTION
- Composition / generic term
- SODIUM BICARBONATE
- Labeler
- Anthea Pharma Private Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250626
- 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 (83854-001-20) / 50 mL in 1 VIAL · 83854-001-20
- 25 VIAL in 1 CARTON (83854-001-25) / 50 mL in 1 VIAL · 83854-001-25
Source and coverage
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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.
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