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IXEMPRA
IXEMPRA - 0015-1910-12 - (ixabepilone)
Drug Information of IXEMPRA
| Product NDC: | 0015-1910 |
| Proprietary Name: | IXEMPRA |
| Non Proprietary Name: | ixabepilone |
| Active Ingredient(s): | & nbsp; ixabepilone |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IXEMPRA
| Product NDC: | 0015-1910 |
| Labeler Name: | E.R. Squibb & Sons, L.L.C. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022065 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20071016 |
Package Information of IXEMPRA
| Package NDC: | 0015-1910-12 |
| Package Description: | 1 KIT in 1 PACKAGE, COMBINATION (0015-1910-12) * 8 mL in 1 VIAL, SINGLE-USE * 8 mL in 1 VIAL, SINGLE-USE |
NDC Information of IXEMPRA
| NDC Code | 0015-1910-12 |
| Proprietary Name | IXEMPRA |
| Package Description | 1 KIT in 1 PACKAGE, COMBINATION (0015-1910-12) * 8 mL in 1 VIAL, SINGLE-USE * 8 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0015-1910 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ixabepilone |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20071016 |
| Marketing Category Name | NDA |
| Labeler Name | E.R. Squibb & Sons, L.L.C. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
