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SPRYCEL
SPRYCEL - 54868-5759-0 - (dasatinib)
Drug Information of SPRYCEL
| Product NDC: | 54868-5759 |
| Proprietary Name: | SPRYCEL |
| Non Proprietary Name: | dasatinib |
| Active Ingredient(s): | 70 mg/1 & nbsp; dasatinib |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SPRYCEL
| Product NDC: | 54868-5759 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021986 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070212 |
Package Information of SPRYCEL
| Package NDC: | 54868-5759-0 |
| Package Description: | 1 BOTTLE in 1 CARTON (54868-5759-0) > 60 TABLET in 1 BOTTLE |
NDC Information of SPRYCEL
| NDC Code | 54868-5759-0 |
| Proprietary Name | SPRYCEL |
| Package Description | 1 BOTTLE in 1 CARTON (54868-5759-0) > 60 TABLET in 1 BOTTLE |
| Product NDC | 54868-5759 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dasatinib |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070212 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | DASATINIB |
| Strength Number | 70 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
