Class II · Moderate risk
Doxycycline Hyclate tablets USP
Failed dissolution specifications
National Drug Code
Is NDC 55289-0866-87 recalled?
Doxycycline · 300 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-866-87)
Yes — this exact package was recalled
2 FDA recalls name the code 55289-0866-87 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, Coated · Oral
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 55289-0866
Recalls naming this package
Class II · Moderate risk
Doxycycline Hyclate USP Tablets
Failed Dissolution Specifications: manufacturer West-Ward Pharm Corp. recalled these repackaged lots due to failed dissolution results.
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
- 55289-0791 Phentermine Hydrochloride 2
- 55289-0274 See recall 1
- 55289-0673 See recall 1
- 55289-0765 See recall 1
- 55289-0964 See recall 1
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