Class II · Moderate risk
Levothyroxine Sodium Tablets
Subpotent Drug
National Drug Code
Is NDC 16729-0450-17 recalled?
Levothyroxine sodium · 1000 TABLET in 1 BOTTLE (16729-450-17)
Yes — this exact package was recalled
2 FDA recalls name the code 16729-0450-17 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.
3 of these recalls are still ongoing.
- Active ingredient
- Levothyroxine Sodium
- Strength
- LEVOTHYROXINE SODIUM 88 ug/1
- Form
- Tablet · Oral
- Labeler
- Accord Healthcare Inc.
- Type
- Human Prescription Drug
- Product code
- 16729-0450
Recalls naming this package
Class II · Moderate risk
Levothyroxine Sodium Tablets
Subpotent: During long term stability testing of Levothyroxine Sodium Tablets USP for 88 mcg, the assay content was observed below the approved specification range.
Class II · Moderate risk
Levothyroxine Sodium Tablets
Subpotent
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
- 16729-0452 Levothyroxine sodium 3
- 16729-0182 Hydrochlorothiazide 2
- 16729-0434 Daptomycin 2
- 16729-0449 Levothyroxine sodium 2
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.