NDC 64725-3920
Geodon 20 mg per 1 mL injection, powder, lyophilized, for solution
On the label: TYA Pharmaceuticals. It's repackaged: TYA Pharmaceuticals rebottles it from Roerig's NDC 0049-3920.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Roerig names for other drugs.
Repackaging site
- TYA Pharmaceuticals, Location not on file · repackages it and relabels it
Recalls
- Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
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
- injection, powder, lyophilized, for solution
- Strength
- 20 mg per 1 mL
- Approval
- NDA NDA020919
- On the market since
- Dec 23, 2003
- Package NDCs
64725-3920-1- Official label
- DailyMed (National Library of Medicine), updated Aug 13, 2014
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?