Tacrolimus
- Product NDC
- 70518-2124
- 11-digit product format
- 705182124
- Labeler code
- 70518
- Product ID
- 70518-2124_dad321ee-e694-1c51-e053-2a95a90a1015
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tacrolimus
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091195
- Marketing category
- ANDA
- Marketing start
- 2019-05-29
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-2124-0 | 70518212400 | 30 CAPSULE in 1 BLISTER PACK (70518-2124-0) | 30 capsule | 2019-05-29 | 0000-00-00 | No | No | Current |
| 70518-2124-1 | 70518212401 | 100 POUCH in 1 BOX (70518-2124-1) > 1 CAPSULE in 1 POUCH (70518-2124-2) | 100 pouch | 2021-02-09 | 0000-00-00 | No | No | Current |