Tacrolimus
- Product NDC
- 0781-9303
- 11-digit product format
- 007819303
- Labeler code
- 0781
- Product ID
- 0781-9303_9d5be1ff-0d4e-47a8-92f4-6a359e623045
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tacrolimus
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA065461
- Marketing category
- ANDA
- Marketing start
- 2012-01-15
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record