United States · FDA National Drug Code directory
Prochlorperazine
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
- 0713-0135_462a6c34-db6d-8d31-e063-6294a90ae196
- Product NDC
- 0713-0135
- Form
- SUPPOSITORY
- Composition / generic term
- Prochlorperazine
- Labeler
- Cosette Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19931130
- Source listing expiry
- 20261231
Source-listed ingredients
- PROCHLORPERAZINE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 BLISTER PACK in 1 CARTON (0713-0135-10) / 1 SUPPOSITORY in 1 BLISTER PACK · 0713-0135-10
- 12 BLISTER PACK in 1 CARTON (0713-0135-12) / 1 SUPPOSITORY in 1 BLISTER PACK · 0713-0135-12
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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