United States · FDA National Drug Code directory
PROCHLORPERAZINE EDISYLATE
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
- 25021-790_18174b35-89ba-487a-bbc5-95716b8c1274
- Product NDC
- 25021-790
- Form
- INJECTION
- Composition / generic term
- PROCHLORPERAZINE EDISYLATE
- Labeler
- Sagent Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211115
- Source listing expiry
- 20261231
Source-listed ingredients
- PROCHLORPERAZINE EDISYLATE — 5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (25021-790-02) / 2 mL in 1 VIAL · 25021-790-02
- 25 VIAL in 1 CARTON (25021-790-03) / 2 mL in 1 VIAL · 25021-790-03
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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