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DOCEFREZ
DOCEFREZ - 47335-286-41 - (docetaxel anhydrous)
Drug Information of DOCEFREZ
| Product NDC: | 47335-286 |
| Proprietary Name: | DOCEFREZ |
| Non Proprietary Name: | docetaxel anhydrous |
| Active Ingredient(s): | & nbsp; docetaxel anhydrous |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOCEFREZ
| Product NDC: | 47335-286 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022534 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110503 |
Package Information of DOCEFREZ
| Package NDC: | 47335-286-41 |
| Package Description: | 1 KIT in 1 CARTON (47335-286-41) * 1 mL in 1 VIAL, SINGLE-USE * 4.21 mL in 1 VIAL, SINGLE-USE (47335-288-40) |
NDC Information of DOCEFREZ
| NDC Code | 47335-286-41 |
| Proprietary Name | DOCEFREZ |
| Package Description | 1 KIT in 1 CARTON (47335-286-41) * 1 mL in 1 VIAL, SINGLE-USE * 4.21 mL in 1 VIAL, SINGLE-USE (47335-288-40) |
| Product NDC | 47335-286 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | docetaxel anhydrous |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110503 |
| Marketing Category Name | NDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
