Tacrolimus
- Product NDC
- 72572-760
- 11-digit product format
- 725720760
- Labeler code
- 72572
- Product ID
- 72572-760_e378bc63-a845-478f-9ca6-235ebf6d318c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tacrolimus
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Civica, Inc.
- Application
- ANDA065461
- Marketing category
- ANDA
- Marketing start
- 2022-01-13
- Marketing end
- 0000-00-00
- Substance
- TACROLIMUS
- Active strength
- 1 mg/1
- Pharmacologic classes
- Calcineurin Inhibitor Immunosuppressant [EPC], Calcineurin Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72572-760-01 | 72572076001 | 100 CAPSULE in 1 BOTTLE (72572-760-01) | 100 capsule | 2022-01-13 | 0000-00-00 | No | No | Current |