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Prograf
Prograf - 21695-170-00 - (Tacrolimus)
Drug Information of Prograf
| Product NDC: | 21695-170 |
| Proprietary Name: | Prograf |
| Non Proprietary Name: | Tacrolimus |
| Active Ingredient(s): | 1 mg/1 & nbsp; Tacrolimus |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, GELATIN COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prograf
| Product NDC: | 21695-170 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050708 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19940408 |
Package Information of Prograf
| Package NDC: | 21695-170-00 |
| Package Description: | 1 BOTTLE in 1 CARTON (21695-170-00) > 100 CAPSULE, GELATIN COATED in 1 BOTTLE |
NDC Information of Prograf
| NDC Code | 21695-170-00 |
| Proprietary Name | Prograf |
| Package Description | 1 BOTTLE in 1 CARTON (21695-170-00) > 100 CAPSULE, GELATIN COATED in 1 BOTTLE |
| Product NDC | 21695-170 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tacrolimus |
| Dosage Form Name | CAPSULE, GELATIN COATED |
| Route Name | ORAL |
| Start Marketing Date | 19940408 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | ANHYDROUS TACROLIMUS |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
