Tacrolimus
- Product NDC
- 72189-536
- 11-digit product format
- 721890536
- Labeler code
- 72189
- Product ID
- 72189-536_13278868-e3cb-d2d0-e063-6294a90a6533
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tacrolimus
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA065461
- Marketing category
- ANDA
- Marketing start
- 2024-02-07
- Substance
- TACROLIMUS
- Active strength
- 1 mg/1
- Pharmacologic classes
- Calcineurin Inhibitor Immunosuppressant [EPC], Calcineurin Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| WM0HAQ4WNM | TACROLIMUS | 109581-93-3 | TACROLIMUS |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-536-30 | 72189053630 | 30 CAPSULE in 1 BOTTLE (72189-536-30) | 30 capsule | 2024-02-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Tacrolimus | Direct_Rx | 2024-03-08 | HUMAN PRESCRIPTION DRUG LABEL | 3 |