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DOCETAXEL
DOCETAXEL - 16729-120-49 - (docetaxel)
Drug Information of DOCETAXEL
| Product NDC: | 16729-120 |
| Proprietary Name: | DOCETAXEL |
| Non Proprietary Name: | docetaxel |
| Active Ingredient(s): | & nbsp; docetaxel |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOCETAXEL
| Product NDC: | 16729-120 |
| Labeler Name: | Accord Healthcare Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA201195 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110630 |
Package Information of DOCETAXEL
| Package NDC: | 16729-120-49 |
| Package Description: | 1 KIT in 1 CARTON (16729-120-49) * .5 mL in 1 VIAL, SINGLE-USE * 1.95 mL in 1 VIAL, SINGLE-USE |
NDC Information of DOCETAXEL
| NDC Code | 16729-120-49 |
| Proprietary Name | DOCETAXEL |
| Package Description | 1 KIT in 1 CARTON (16729-120-49) * .5 mL in 1 VIAL, SINGLE-USE * 1.95 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 16729-120 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | docetaxel |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110630 |
| Marketing Category Name | NDA |
| Labeler Name | Accord Healthcare Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
