Details for New Drug Application (NDA): 204117
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The generic ingredient in ZIPRASIDONE HYDROCHLORIDE is ziprasidone hydrochloride. There are twenty-three drug master file entries for this compound. Twenty-three suppliers are listed for this compound. Additional details are available on the ziprasidone hydrochloride profile page.
Summary for 204117
Tradename: | ZIPRASIDONE HYDROCHLORIDE |
Applicant: | Aurobindo Pharma |
Ingredient: | ziprasidone hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 204117
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ZIPRASIDONE HYDROCHLORIDE | ziprasidone hydrochloride | CAPSULE;ORAL | 204117 | ANDA | Aurobindo Pharma Limited | 65862-702 | 65862-702-60 | 60 CAPSULE in 1 BOTTLE (65862-702-60) |
ZIPRASIDONE HYDROCHLORIDE | ziprasidone hydrochloride | CAPSULE;ORAL | 204117 | ANDA | Aurobindo Pharma Limited | 65862-702 | 65862-702-80 | 8 BLISTER PACK in 1 CARTON (65862-702-80) / 10 CAPSULE in 1 BLISTER PACK (65862-702-10) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 20MG BASE | ||||
Approval Date: | Dec 27, 2016 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 40MG BASE | ||||
Approval Date: | Dec 27, 2016 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 60MG BASE | ||||
Approval Date: | Dec 27, 2016 | TE: | AB | RLD: | No |
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