Class II · Moderate risk
Endometrin
cGMP deviations: potential for Microbial Contamination of Non-Sterile Products
National Drug Code
Is NDC 55566-6500-03 recalled?
Endometrin · 1 CARTON in 1 CARTON (55566-6500-3) / 21 BLISTER PACK in 1 CARTON (55566-6500-2) / 1 INSERT in 1 BLISTER PACK (55566-6500-1)
Yes — this exact package was recalled
2 FDA recalls name the code 55566-6500-03 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
- Progesterone
- Strength
- PROGESTERONE 100 mg/1
- Form
- Insert · Vaginal
- Labeler
- Ferring Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 55566-6500
Recalls naming this package
Class III · Low risk
Endometrin
Discoloration; due to prolonged heat exposure.
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
- 55566-1000 See recall 1
- 55566-1010 Fyremadel 1
- 55566-1501 See recall 1
- 55566-2500 See recall 1
- 55566-7501 Menopur 1
- 55566-8303 Firmagon 1
Free recall alerts
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