Ziprasidone is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Greenstone Llc. The primary component is Ziprasidone Hydrochloride.
Product ID | 59762-1006_542dce3e-ccac-4526-b715-090b07b54cfa |
NDC | 59762-1006 |
Product Type | Human Prescription Drug |
Proprietary Name | Ziprasidone |
Generic Name | Ziprasidone |
Dosage Form | Capsule |
Route of Administration | ORAL |
Marketing Start Date | 2021-11-03 |
Marketing Category | NDA AUTHORIZED GENERIC / |
Application Number | NDA020825 |
Labeler Name | Greenstone LLC |
Substance Name | ZIPRASIDONE HYDROCHLORIDE |
Active Ingredient Strength | 20 mg/1 |
Pharm Classes | Atypical Antipsychotic [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2021-11-03 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
59762-1006 | Ziprasidone | ziprasidone |
59762-2001 | Ziprasidone | ziprasidone hydrochloride |
59762-2002 | Ziprasidone | ziprasidone hydrochloride |
59762-2003 | Ziprasidone | ziprasidone hydrochloride |
59762-2004 | Ziprasidone | ziprasidone hydrochloride |
68382-237 | Ziprasidone | Ziprasidone |
68382-238 | Ziprasidone | Ziprasidone |
68382-239 | Ziprasidone | Ziprasidone |
68382-240 | Ziprasidone | Ziprasidone |
69189-2003 | Ziprasidone | Ziprasidone |
70771-1182 | Ziprasidone | Ziprasidone |
70771-1181 | Ziprasidone | Ziprasidone |
70771-1180 | Ziprasidone | Ziprasidone |
70771-1179 | Ziprasidone | Ziprasidone |
72578-022 | Ziprasidone | Ziprasidone |
72578-021 | Ziprasidone | Ziprasidone |
72578-020 | Ziprasidone | Ziprasidone |
72578-023 | Ziprasidone | Ziprasidone |
0049-0352 | Geodon | ziprasidone |
0049-0356 | Geodon | ziprasidone |
0049-0358 | Geodon | ziprasidone |