Class II · Moderate risk
DOXYCYCLINE HYCLATE Tablet
Labeling: Label Mixup; DOXYCYCLINE HYCLATE, Tablet, 100 mg may be potentially mislabeled as DESLORATADINE, Tablet, 5 mg, NDC 00085126401, Pedigree: AD30993_5, EXP: 2/28/2014.
National Drug Code
Is NDC 53489-0120-02 recalled?
Doxycycline Hyclate · 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-120-02)
Yes — this exact package was recalled
1 FDA recall names the code 53489-0120-02 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
- Doxycycline Hyclate
- Strength
- DOXYCYCLINE HYCLATE 100 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 53489-0120
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
- 53489-0146 Sulfamethoxazole and Trimethoprim 2
- 53489-0677 See recall 2
- 53489-0678 See recall 2
- 53489-0143 Spironolactone 1
- 53489-0215 See recall 1
- 53489-0216 See recall 1
Free recall alerts
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