Inactive ingredient entry
ANHYDROUS LACTOSE · ORAL CAPSULE, DELAYED RELEASE
FDA Inactive Ingredient Database · UNII 3SY5LH9PMK
Key facts
| Inactive ingredient | ANHYDROUS LACTOSE |
|---|---|
| Route | ORAL |
| Dosage form | CAPSULE, DELAYED RELEASE |
| Maximum daily exposure (MDE) | 360 mg |
| UNII | 3SY5LH9PMK |
| CAS registry number | 16984-38-6 |
At a glance
- 10–99 Routes and dosage forms listed for this ingredient
- 10–99 IID entries for this UNII (all names)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA Inactive Ingredient Database
The FDA Inactive Ingredient Database lists excipients in approved drug products by route and dosage form, with the highest potency per unit dose and, where published, the maximum daily exposure.
Source: U.S. Food and Drug Administration (FDA), Inactive Ingredient Database (IID)