Home
>
National Drug Code (NDC)
>
Ziprasidone
Ziprasidone - 59762-2004-2 - (ziprasidone hydrochloride)
Drug Information of Ziprasidone
| Product NDC: | 59762-2004 |
| Proprietary Name: | Ziprasidone |
| Non Proprietary Name: | ziprasidone hydrochloride |
| Active Ingredient(s): | 80 mg/1 & nbsp; ziprasidone hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ziprasidone
| Product NDC: | 59762-2004 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020825 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20010205 |
Package Information of Ziprasidone
| Package NDC: | 59762-2004-2 |
| Package Description: | 500 CAPSULE in 1 BOTTLE (59762-2004-2) |
NDC Information of Ziprasidone
| NDC Code | 59762-2004-2 |
| Proprietary Name | Ziprasidone |
| Package Description | 500 CAPSULE in 1 BOTTLE (59762-2004-2) |
| Product NDC | 59762-2004 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ziprasidone hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20010205 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | ZIPRASIDONE HYDROCHLORIDE |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC] |
