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Ziprasidone Hydrochloride
Ziprasidone Hydrochloride - 0904-6270-08 - (Ziprasidone Hydrochloride)
Drug Information of Ziprasidone Hydrochloride
| Product NDC: | 0904-6270 |
| Proprietary Name: | Ziprasidone Hydrochloride |
| 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 Ziprasidone Hydrochloride
| Product NDC: | 0904-6270 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077565 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120315 |
Package Information of Ziprasidone Hydrochloride
| Package NDC: | 0904-6270-08 |
| Package Description: | 40 CAPSULE in 1 BOX, UNIT-DOSE (0904-6270-08) |
NDC Information of Ziprasidone Hydrochloride
| NDC Code | 0904-6270-08 |
| Proprietary Name | Ziprasidone Hydrochloride |
| Package Description | 40 CAPSULE in 1 BOX, UNIT-DOSE (0904-6270-08) |
| Product NDC | 0904-6270 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ziprasidone Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120315 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | ZIPRASIDONE HYDROCHLORIDE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC] |
