NDC 70518-2925

Ziprasidone

Ziprasidone Hydrochloride

Ziprasidone is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Ziprasidone Hydrochloride.

Product ID70518-2925_d423dcbe-0ab7-804c-e053-2a95a90a5047
NDC70518-2925
Product TypeHuman Prescription Drug
Proprietary NameZiprasidone
Generic NameZiprasidone Hydrochloride
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2020-10-27
Marketing CategoryNDA AUTHORIZED GENERIC /
Application NumberNDA020825
Labeler NameREMEDYREPACK INC.
Substance NameZIPRASIDONE HYDROCHLORIDE
Active Ingredient Strength20 mg/1
Pharm ClassesAtypical Antipsychotic [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 70518-2925-0

30 POUCH in 1 BOX (70518-2925-0) > 1 CAPSULE in 1 POUCH (70518-2925-1)
Marketing Start Date2020-10-27
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Ziprasidone" or generic name "Ziprasidone Hydrochloride"

NDCBrand NameGeneric Name
68382-238ZiprasidoneZiprasidone
68382-239ZiprasidoneZiprasidone
68382-237ZiprasidoneZiprasidone
68382-240ZiprasidoneZiprasidone
69189-2003ZiprasidoneZiprasidone
70771-1182ZiprasidoneZiprasidone
70771-1181ZiprasidoneZiprasidone
70771-1180ZiprasidoneZiprasidone
70771-1179ZiprasidoneZiprasidone
59762-2004ZiprasidoneZiprasidone
59762-2001ZiprasidoneZiprasidone
59762-2002ZiprasidoneZiprasidone
59762-2003ZiprasidoneZiprasidone
72578-022ZiprasidoneZiprasidone
72578-021ZiprasidoneZiprasidone
72578-020ZiprasidoneZiprasidone
72578-023ZiprasidoneZiprasidone
0049-0052Geodonziprasidone hydrochloride
0049-0054Geodonziprasidone hydrochloride
0049-0056Geodonziprasidone hydrochloride
0049-0058Geodonziprasidone hydrochloride
0049-0352Geodonziprasidone
0049-0356Geodonziprasidone
0049-0358Geodonziprasidone
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