Class II · Moderate risk
Isotretinoin Capsules
Superpotent and Subpotent
National Drug Code
Is NDC 0591-2436-15 recalled?
Isotretinoin · 3 BLISTER PACK in 1 CARTON (0591-2436-15) / 10 CAPSULE in 1 BLISTER PACK (0591-2436-45)
Yes — this exact package was recalled
2 FDA recalls name the code 0591-2436-15 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.
2 of these recalls are still ongoing.
- Active ingredient
- Isotretinoin
- Strength
- ISOTRETINOIN 40 mg/1
- Form
- Capsule · Oral
- Labeler
- Actavis Pharma, Inc.
- Type
- Human Prescription Drug
- Product code
- 0591-2436
Recalls naming this package
Class II · Moderate risk
Isotretinoin Capsules
Superpotent Drug: The 3-month stability result for assay was found to be above specification limit
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
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