Details for New Drug Application (NDA): 208988
✉ Email this page to a colleague
The generic ingredient in ZIPRASIDONE HYDROCHLORIDE is ziprasidone hydrochloride. There are twenty-three drug master file entries for this compound. Twenty-two suppliers are listed for this compound. Additional details are available on the ziprasidone hydrochloride profile page.
Summary for 208988
Tradename: | ZIPRASIDONE HYDROCHLORIDE |
Applicant: | Zydus Lifesciences |
Ingredient: | ziprasidone hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 208988
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ZIPRASIDONE HYDROCHLORIDE | ziprasidone hydrochloride | CAPSULE;ORAL | 208988 | ANDA | Zydus Lifesciences Limited | 70771-1179 | 70771-1179-5 | 500 CAPSULE in 1 BOTTLE (70771-1179-5) |
ZIPRASIDONE HYDROCHLORIDE | ziprasidone hydrochloride | CAPSULE;ORAL | 208988 | ANDA | Zydus Lifesciences Limited | 70771-1179 | 70771-1179-6 | 60 CAPSULE in 1 BOTTLE (70771-1179-6) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 20MG BASE | ||||
Approval Date: | Aug 22, 2017 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 40MG BASE | ||||
Approval Date: | Aug 22, 2017 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 60MG BASE | ||||
Approval Date: | Aug 22, 2017 | TE: | AB | RLD: | No |
Complete Access Available with Subscription