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Prochlorperazine Edisylate

NDC 0713-0351 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerCosette Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213626
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsPROCHLORPERAZINE EDISYLATE (5 mg/mL)
Marketing started20220211
Package count2

External sources

Source: openFDA. Public-domain (CC0).