| Product NDC: | 35356-097 | 
| Proprietary Name: | Geodon | 
| 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) | 
| Product NDC: | 35356-097 | 
| Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA020825 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 20010205 | 
| Package NDC: | 35356-097-60 | 
| Package Description: | 60 CAPSULE in 1 BOTTLE (35356-097-60) | 
| NDC Code | 35356-097-60 | 
| Proprietary Name | Geodon | 
| Package Description | 60 CAPSULE in 1 BOTTLE (35356-097-60) | 
| Product NDC | 35356-097 | 
| 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 | 
| Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 
| Substance Name | ZIPRASIDONE HYDROCHLORIDE | 
| Strength Number | 80 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC] |