Class II ยท Moderate risk
Finasteride Tablets USP
CGMP Deviations: recalling drug products following an FDA inspection.
National Drug Code
Is NDC 16729-0090-01 recalled?
Finasteride · 100 TABLET, FILM COATED in 1 BOTTLE (16729-090-01)
Yes — this exact package was recalled
1 FDA recall names the code 16729-0090-01 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
- finasteride
- Strength
- FINASTERIDE 5 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Accord Healthcare, Inc.
- Type
- Human Prescription Drug
- Product code
- 16729-0090
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
- 16729-0447 Levothyroxine sodium 4
- 16729-0448 Levothyroxine sodium 3
- 16729-0450 Levothyroxine sodium 3
- 16729-0452 Levothyroxine sodium 3
- 16729-0182 Hydrochlorothiazide 2
- 16729-0434 Daptomycin 2
Free recall alerts
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