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Tacrolimus
Tacrolimus - 16729-042-01 - (Tacrolimus)
Drug Information of Tacrolimus
| Product NDC: | 16729-042 |
| Proprietary Name: | Tacrolimus |
| Non Proprietary Name: | Tacrolimus |
| Active Ingredient(s): | 1 mg/1 & nbsp; Tacrolimus |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tacrolimus
| Product NDC: | 16729-042 |
| Labeler Name: | Accord Heathcare, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091195 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110615 |
Package Information of Tacrolimus
| Package NDC: | 16729-042-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (16729-042-01) |
NDC Information of Tacrolimus
| NDC Code | 16729-042-01 |
| Proprietary Name | Tacrolimus |
| Package Description | 100 CAPSULE in 1 BOTTLE (16729-042-01) |
| Product NDC | 16729-042 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tacrolimus |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110615 |
| Marketing Category Name | ANDA |
| Labeler Name | Accord Heathcare, Inc. |
| Substance Name | TACROLIMUS |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA] |
