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Geodon
Geodon - 21695-061-15 - (ziprasidone hydrochloride)
Drug Information of Geodon
| Product NDC: | 21695-061 |
| Proprietary Name: | Geodon |
| Non Proprietary Name: | ziprasidone hydrochloride |
| Active Ingredient(s): | 40 mg/1 & nbsp; ziprasidone hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Geodon
| Product NDC: | 21695-061 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020825 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010205 |
Package Information of Geodon
| Package NDC: | 21695-061-15 |
| Package Description: | 15 CAPSULE in 1 BOTTLE (21695-061-15) |
NDC Information of Geodon
| NDC Code | 21695-061-15 |
| Proprietary Name | Geodon |
| Package Description | 15 CAPSULE in 1 BOTTLE (21695-061-15) |
| Product NDC | 21695-061 |
| 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 | Rebel Distributors Corp |
| Substance Name | ZIPRASIDONE HYDROCHLORIDE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC] |
