Tacrolimus
- Product NDC
- 69452-154
- 11-digit product format
- 694520154
- Labeler code
- 69452
- Product ID
- 69452-154_b748f1a3-f852-4326-e053-2995a90ac2c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tacrolimus
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- BionPharma Inc.,
- Application
- ANDA090802
- Marketing category
- ANDA
- Marketing start
- 2016-02-26
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69452-154-20 | 69452015420 | 100 CAPSULE, GELATIN COATED in 1 BOTTLE (69452-154-20) | 2016-02-26 | 0000-00-00 | No | No | Current |