Details for New Drug Application (NDA): 204117
✉ Email this page to a colleague
NDA 204117 describes ZIPRASIDONE HYDROCHLORIDE, which is a drug marketed by Apotex, Aurobindo Pharma, Chartwell Rx, Dr Reddys Labs Inc, Lupin Pharms, Macleods Pharms Ltd, Mylan, Sandoz Inc, and Zydus Lifesciences, and is included in nine NDAs. It is available from twenty suppliers. Additional details are available on the ZIPRASIDONE HYDROCHLORIDE profile page.
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.
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 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 | ||||
Complete Access Available with Subscription
