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Last Updated: December 22, 2024

Details for New Drug Application (NDA): 214192


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NDA 214192 describes PROCHLORPERAZINE EDISYLATE, which is a drug marketed by Morton Grove, Amneal, Avet Lifesciences, Caplin, Eugia Pharma, Gland Pharma Ltd, Hikma, Hospira, Marsam Pharms Llc, Mylan Labs Ltd, Nexus, Sagent, Smith And Nephew, Somerset Theraps Llc, Teva Parenteral, Viwit Pharm, Watson Labs, Wyeth Ayerst, and Alpharma Us Pharms, and is included in twenty-four NDAs. It is available from seventeen suppliers. Additional details are available on the PROCHLORPERAZINE EDISYLATE profile page.

The generic ingredient in PROCHLORPERAZINE EDISYLATE is prochlorperazine edisylate. There are twenty-one drug master file entries for this compound. Seventeen suppliers are listed for this compound. Additional details are available on the prochlorperazine edisylate profile page.
Summary for 214192
Tradename:PROCHLORPERAZINE EDISYLATE
Applicant:Amneal
Ingredient:prochlorperazine edisylate
Patents:0
Pharmacology for NDA: 214192
Suppliers and Packaging for NDA: 214192
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
PROCHLORPERAZINE EDISYLATE prochlorperazine edisylate INJECTABLE;INJECTION 214192 ANDA Amneal Pharmaceuticals LLC 70121-1580 70121-1580-5 25 VIAL in 1 CARTON (70121-1580-5) / 2 mL in 1 VIAL (70121-1580-1)
PROCHLORPERAZINE EDISYLATE prochlorperazine edisylate INJECTABLE;INJECTION 214192 ANDA Amneal Pharmaceuticals LLC 70121-1580 70121-1580-7 10 VIAL in 1 CARTON (70121-1580-7) / 2 mL in 1 VIAL (70121-1580-1)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 5MG BASE/ML
Approval Date:Nov 28, 2022TE:APRLD:No

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