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Geodon
Geodon - 0049-3920-83 - (ZIPRASIDONE MESYLATE)
Drug Information of Geodon
| Product NDC: | 0049-3920 |
| Proprietary Name: | Geodon |
| Non Proprietary Name: | ZIPRASIDONE MESYLATE |
| Active Ingredient(s): | 20 mg/mL & nbsp; ZIPRASIDONE MESYLATE |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Geodon
| Product NDC: | 0049-3920 |
| Labeler Name: | Roerig |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020919 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20031223 |
Package Information of Geodon
| Package NDC: | 0049-3920-83 |
| Package Description: | 1 mL in 1 VIAL, SINGLE-DOSE (0049-3920-83) |
NDC Information of Geodon
| NDC Code | 0049-3920-83 |
| Proprietary Name | Geodon |
| Package Description | 1 mL in 1 VIAL, SINGLE-DOSE (0049-3920-83) |
| Product NDC | 0049-3920 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ZIPRASIDONE MESYLATE |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20031223 |
| Marketing Category Name | NDA |
| Labeler Name | Roerig |
| Substance Name | ZIPRASIDONE MESYLATE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC] |
