NDC 0904-6270
Ziprasidone 40 mg capsule
On the label: Major Pharmaceuticals. It's repackaged: Major Pharmaceuticals rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-257.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Recalls
- May 31, 2023 · Class I · The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone Hydrochloride Capsules, 20 mg were found to contain blister packages labeled as and containing Dronabinol Capsules, USP, 2.5 mg.
Lots: Lot: T04769 Exp. 2024/12
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ziprasidone: every company that makes it
- Form
- capsule, oral
- Strength
- 40 mg
- Approval
- ANDA ANDA077565
- On the market since
- Mar 15, 2012
- Package NDCs
0904-6270-080904-6270-45- Official label
- DailyMed (National Library of Medicine), updated Jun 9, 2026
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