Tacrolimus
- Product NDC
- 70518-2593
- 11-digit product format
- 705182593
- Labeler code
- 70518
- Product ID
- 70518-2593_ca7776bf-3b7a-7289-e053-2995a90a6591
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tacrolimus
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065461
- Marketing category
- ANDA
- Marketing start
- 2020-03-03
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2593-0 | 70518259300 | 30 CAPSULE in 1 BLISTER PACK (70518-2593-0) | 30 capsule | 2020-03-03 | 0000-00-00 | No | No | Current |