Class II · Moderate risk
Estriol
Failed Impurities/Degradation Specifications: Additional testing found Out of Specification impurity test results.
National Drug Code
Is NDC 76420-0049-36 recalled?
Estriol · .06 g in 1 JAR (76420-049-36)
Yes — this exact package was recalled
1 FDA recall names the code 76420-0049-36 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
- Estriol
- Strength
- ESTRIOL 1 g/g
- Form
- Powder
- Labeler
- Asclemed USA, Inc.
- Type
- Bulk Ingredient
- Product code
- 76420-0049
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
- 76420-0634 Duloxetine 1
- 76420-0715 Accucaine 1
- 76420-0750 Dyural 40 Kit 1
- 76420-0755 Dyural 80 Kit 1
- 76420-0760 Lidolog Kit 1
Free recall alerts
Know the day your medication is recalled
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