Class II · Moderate risk
Combipatch
Failed Stability Specifications; out of specification for shear.
National Drug Code
Is NDC 68968-0525-08 recalled?
CombiPatch (estradiol/norethindrone acetate transdermal system) · 8 POUCH in 1 CARTON (68968-0525-8) / 1 PATCH in 1 POUCH / 3.5 d in 1 PATCH
Yes — this exact package was recalled
1 FDA recall names the code 68968-0525-08 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.
1 of these recalls is still ongoing.
- Active ingredient
- estradiol/norethindrone acetate transdermal system
- Strength
- ESTRADIOL .05 mg/d; NORETHINDRONE ACETATE .25 mg/d
- Form
- Patch, Extended Release · Transdermal
- Labeler
- Noven Therapeutics, LLC
- Type
- Human Prescription Drug
- Product code
- 68968-0525
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
- 68968-5554 Daytrana 12
- 68968-5552 Daytrana 11
- 68968-5555 Daytrana 11
- 68968-5553 Daytrana 8
- 68968-6610 Minivelle 3
- 68968-6650 Minivelle 2
Free recall alerts
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