Details for New Drug Application (NDA): 213873
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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 213873
Tradename: | PROCHLORPERAZINE EDISYLATE |
Applicant: | Eugia Pharma |
Ingredient: | prochlorperazine edisylate |
Patents: | 0 |
Suppliers and Packaging for NDA: 213873
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PROCHLORPERAZINE EDISYLATE | prochlorperazine edisylate | INJECTABLE;INJECTION | 213873 | ANDA | Eugia US LLC | 55150-360 | 55150-360-01 | 1 VIAL, MULTI-DOSE in 1 CARTON (55150-360-01) / 2 mL in 1 VIAL, MULTI-DOSE |
PROCHLORPERAZINE EDISYLATE | prochlorperazine edisylate | INJECTABLE;INJECTION | 213873 | ANDA | Eugia US LLC | 55150-360 | 55150-360-25 | 25 VIAL, MULTI-DOSE in 1 CARTON (55150-360-25) / 2 mL in 1 VIAL, MULTI-DOSE |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 5MG BASE/ML | ||||
Approval Date: | Jul 14, 2022 | TE: | AP | RLD: | No |
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