| NDC Code: |
41616-882 |
| Proprietary Name: |
NICARdipine Hydrochloride |
| Suffix: |
|
| Non-Proprietary Name: |
NICARdipine Hydrochloride |
| Dosage Form: |
INJECTION |
| Method: |
INTRAVENOUS |
| Original Marketing Date: |
17-11-2009 |
| Category Name: |
NDA |
| Application Number: |
NDA078405 |
| Labeler: |
SUN PHARMA GLOBAL INC. |
| Substance Name: |
NICARDIPINE HYDROCHLORIDE |
| Active Numerator Strength: |
2.5 |
| Active Ingredient Unit: |
mg/mL |
| Pharm Classes: |
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
| DEA Schedule: |
|
