Class II ยท Moderate risk
Edex (alprostadil for injection)
Lack of Assurance of Sterility: Defective container resulting in the lack of sterility assurance. ok thanks
National Drug Code
Is NDC 52244-0010-02 recalled?
Edex · 2 BLISTER PACK in 1 CARTON (52244-010-02) / 1 CARTRIDGE in 1 BLISTER PACK / 1 mL in 1 CARTRIDGE
Yes — this exact package was recalled
1 FDA recall names the code 52244-0010-02 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- alprostadil
- Strength
- ALPROSTADIL 10 ug/mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intracavernous
- Labeler
- Endo USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 52244-0010
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 52244-0449 See recall 1
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