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Ziprasidone Hydrochloride
Ziprasidone Hydrochloride - 68084-581-09 - (Ziprasidone Hydrochloride)
Drug Information of Ziprasidone Hydrochloride
| Product NDC: | 68084-581 |
| Proprietary Name: | Ziprasidone Hydrochloride |
| Non Proprietary Name: | Ziprasidone Hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; Ziprasidone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ziprasidone Hydrochloride
| Product NDC: | 68084-581 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077560 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130702 |
Package Information of Ziprasidone Hydrochloride
| Package NDC: | 68084-581-09 |
| Package Description: | 8 BLISTER PACK in 1 CARTON (68084-581-09) > 10 CAPSULE in 1 BLISTER PACK (68084-581-11) |
NDC Information of Ziprasidone Hydrochloride
| NDC Code | 68084-581-09 |
| Proprietary Name | Ziprasidone Hydrochloride |
| Package Description | 8 BLISTER PACK in 1 CARTON (68084-581-09) > 10 CAPSULE in 1 BLISTER PACK (68084-581-11) |
| Product NDC | 68084-581 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ziprasidone Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130702 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | ZIPRASIDONE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC] |
