Tacrolimus
- Product NDC
- 70518-2996
- 11-digit product format
- 705182996
- Labeler code
- 70518
- Product ID
- 70518-2996_d3d25d3a-7a87-c162-e053-2a95a90ad7de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tacrolimus
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA212297
- Marketing category
- ANDA
- Marketing start
- 2021-01-19
- 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 |
|---|
| 70518-2996-0 | 70518299600 | 30 CAPSULE in 1 BLISTER PACK (70518-2996-0) | 30 capsule | 2021-01-19 | 0000-00-00 | No | No | Current |