Class III ยท Low risk
Isotretinoin Capsules
Failed Impurities/Degradation Specifications: Tretinoin levels slightly above specification limits.
National Drug Code
Is NDC 69238-1174-03 recalled?
Isotretinoin · 3 BLISTER PACK in 1 CARTON (69238-1174-3) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69238-1174-1)
Yes — this exact package was recalled
1 FDA recall names the code 69238-1174-03 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
- Isotretinoin
- Strength
- ISOTRETINOIN 10 mg/1
- Form
- Capsule, Liquid Filled · Oral
- Labeler
- Amneal Pharmaceuticals LLC
- Type
- Human Prescription Drug
- Product code
- 69238-1174
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
- 69238-1605 Methylergonovine Maleate 2
- 69238-1056 Chlorpromazine Hydrochloride 1
- 69238-1058 Chlorpromazine Hydrochloride 1
- 69238-1060 Chlorpromazine Hydrochloride 1
- 69238-1062 Chlorpromazine Hydrochloride 1
- 69238-1273 Oseltamivir Phosphate 1
Free recall alerts
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