NDC 51407-445
Prasugrel 10 mg tablet, film coated
On the label: Golden State Medical Supply, Inc.. It's repackaged: Golden State Medical Supply, Inc. rebottles it from Mylan Pharmaceuticals Inc.'s NDC 0378-5186.
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 Mylan Pharmaceuticals Inc. names for other drugs.
Repackaging site
- Golden State Medical Supply Inc., Camarillo, CA, United States · repackages it and relabels it
Recalls
- Aug 21, 2026 · Class II · Golden State Medical Supply Inc.
Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution
Lots: Lot # GS062298, Exp Date: 09/30/ 2026. - Aug 17, 2026 · Class II · Mylan Pharmaceuticals Inc
Failed Dissolution Specifications; product failed to meet 18-month stability testing acceptance criteria
Lots: Lot #: 3225272, Exp. September 30, 2026 - Mar 5, 2025 · Class II · Golden State Medical Supply Inc.
Failed Dissolution Specifications
Lots: Lot no's: GS059908, GS060228, GS060709, GS061233, GS061704, GS062158, GS062405, Exp.: 04/30/2026 - Feb 25, 2025 · Class II · Mylan Pharmaceuticals Inc
Failed Dissolution Specifications - low dissolution results
Lots: Lot # 3211073, 3211074, 3211075, Exp 4/30/2026 - Oct 18, 2019 · Class II · Mylan Pharmaceuticals Inc.
Failed Dissolution Specification: Low out of specification dissolution results.
Lots: Lot #: 3089793, Exp. Date September 2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Prasugrel: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA205927
- On the market since
- Jul 12, 2017
- Package NDCs
51407-445-30- Official label
- DailyMed (National Library of Medicine), updated Aug 20, 2024
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