# PROCHLORPERAZINE EDISYLATE

NDC: 51662-1558
Generic name: PROCHLORPERAZINE EDISYLATE
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20220615

FDA application: ANDA089903

## Active ingredients

- PROCHLORPERAZINE EDISYLATE: 5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1558"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1558
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e181c18d-32a8-587e-e053-2995a90acc5b