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ziprasidone hydrochloride
ziprasidone hydrochloride - 55111-257-05 - (ziprasidone hydrochloride)
Drug Information of ziprasidone hydrochloride
| Product NDC: | 55111-257 |
| 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: | 55111-257 |
| Labeler Name: | Dr. Reddy's Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077565 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120302 |
Package Information of ziprasidone hydrochloride
| Package NDC: | 55111-257-05 |
| Package Description: | 500 CAPSULE in 1 BOTTLE (55111-257-05) |
NDC Information of ziprasidone hydrochloride
| NDC Code | 55111-257-05 |
| Proprietary Name | ziprasidone hydrochloride |
| Package Description | 500 CAPSULE in 1 BOTTLE (55111-257-05) |
| Product NDC | 55111-257 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ziprasidone hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120302 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr. Reddy's Laboratories Limited |
| Substance Name | ZIPRASIDONE HYDROCHLORIDE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC] |
