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Ziprasidone hydrochloride
Ziprasidone hydrochloride - 64679-991-01 - (Ziprasidone hydrochloride)
Drug Information of Ziprasidone hydrochloride
| Product NDC: | 64679-991 |
| 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: | 64679-991 |
| Labeler Name: | Wockhardt USA LLC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090348 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120901 |
Package Information of Ziprasidone hydrochloride
| Package NDC: | 64679-991-01 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (64679-991-01) |
NDC Information of Ziprasidone hydrochloride
| NDC Code | 64679-991-01 |
| Proprietary Name | Ziprasidone hydrochloride |
| Package Description | 30 CAPSULE in 1 BOTTLE (64679-991-01) |
| Product NDC | 64679-991 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ziprasidone hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120901 |
| Marketing Category Name | ANDA |
| Labeler Name | Wockhardt USA LLC. |
| Substance Name | ZIPRASIDONE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC] |
