Class II ยท Moderate risk
Estriol
cGMP Deviations; manufacturer initiated recall of API product after deficiencies noted during a recent FDA inspection
National Drug Code
Is NDC 38779-0732-04 recalled?
Estriol · 25 g in 1 JAR (38779-0732-4)
Yes — this exact package was recalled
1 FDA recall names the code 38779-0732-04 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
- Medisca Inc.
- Type
- Bulk Ingredient
- Product code
- 38779-0732
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
- 38779-0869 Estradiol 1
- 38779-0891 See recall 1
- 38779-0989 See recall 1
- 38779-1186 See recall 1
- 38779-2261 See recall 1
- 38779-2673 See recall 1
Free recall alerts
Know the day your medication is recalled
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