Home
>
National Drug Code (NDC)
>
zoledronic acid
zoledronic acid - 47335-962-41 - (zoledronic acid)
Drug Information of zoledronic acid
| Product NDC: | 47335-962 |
| Proprietary Name: | zoledronic acid |
| Non Proprietary Name: | zoledronic acid |
| Active Ingredient(s): | & nbsp; zoledronic acid |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of zoledronic acid
| Product NDC: | 47335-962 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090018 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130304 |
Package Information of zoledronic acid
| Package NDC: | 47335-962-41 |
| Package Description: | 1 KIT in 1 CARTON (47335-962-41) * 5 mL in 1 VIAL, SINGLE-DOSE * 5 mL in 1 AMPULE (47335-247-40) |
NDC Information of zoledronic acid
| NDC Code | 47335-962-41 |
| Proprietary Name | zoledronic acid |
| Package Description | 1 KIT in 1 CARTON (47335-962-41) * 5 mL in 1 VIAL, SINGLE-DOSE * 5 mL in 1 AMPULE (47335-247-40) |
| Product NDC | 47335-962 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | zoledronic acid |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130304 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
