Class II · Moderate risk
Diethylpropion
cMGP Deviations: Drug products repackaged into pouches without supporting stability studies.
National Drug Code
Is NDC 0527-1477-01 recalled?
Diethylpropion Hydrochloride ER · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-1477-01)
Yes — this exact package was recalled
1 FDA recall names the code 0527-1477-01 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
- Diethylpropion Hydrochloride
- Strength
- DIETHYLPROPION HYDROCHLORIDE 75 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Lannett Company, Inc.
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 0527-1477
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
- 0527-1632 See recall 3
- 0527-0597 See recall 1
- 0527-0762 Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate 1
- 0527-0790 Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate 1
- 0527-1116 See recall 1
- 0527-1231 Primidone 1
Free recall alerts
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