Class II · Moderate risk
Minocycline HCL
Labeling: Label Mixup: MINOCYCLINE HCL, Capsule, 100 mg may have potentially been mislabeled as the following drug: PROGESTERONE, Capsule, 100 mg, NDC 00591396401, Pedigree: AD73611_4, EXP: 5/30/2014.
National Drug Code
Is NDC 0591-5695-50 recalled?
Minocycline Hydrochloride · 50 CAPSULE in 1 BOTTLE, PLASTIC (0591-5695-50)
Yes — this exact package was recalled
1 FDA recall names the code 0591-5695-50 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
- Minocycline Hydrochloride
- Strength
- MINOCYCLINE HYDROCHLORIDE 100 mg/1
- Form
- Capsule
- Labeler
- Actavis Pharma, Inc.
- Type
- Drug for Further Processing
- Product code
- 0591-5695
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
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