United States · FDA National Drug Code directory
Procainamide Hydrochloride
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
- 0409-1902_8bd73868-f050-4ffb-9bb1-222be0bd3f0f
- Product NDC
- 0409-1902
- Form
- INJECTION, SOLUTION
- Composition / generic term
- PROCAINAMIDE HYDROCHLORIDE
- Labeler
- Hospira, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20060308
- Source listing expiry
- 20271231
Source-listed ingredients
- PROCAINAMIDE HYDROCHLORIDE — 100 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 CARTON in 1 CASE (0409-1902-01) / 1 VIAL, MULTI-DOSE in 1 CARTON (0409-1902-11) / 10 mL in 1 VIAL, MULTI-DOSE · 0409-1902-01
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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