Tacrolimus
- Product NDC
- 70518-3022
- 11-digit product format
- 705183022
- Labeler code
- 70518
- Product ID
- 70518-3022_bcccde3e-f9ff-415c-e053-2995a90acf78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tacrolimus
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA212297
- Marketing category
- ANDA
- Marketing start
- 2021-02-11
- 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 |
|---|
| 70518-3022-0 | 70518302200 | 100 POUCH in 1 BOX (70518-3022-0) > 1 CAPSULE in 1 POUCH (70518-3022-1) | 100 pouch | 2021-02-11 | 0000-00-00 | No | No | Current |