| NDC Code: |
0185-7322 |
| Proprietary Name: |
Ipratropium Bromide and Albuterol Sulfate |
| Suffix: |
|
| Non-Proprietary Name: |
ipratropium bromide and albuterol sulfate |
| Dosage Form: |
SOLUTION |
| Method: |
RESPIRATORY (INHALATION) |
| Original Marketing Date: |
21-03-2001 |
| Category Name: |
NDA |
| Application Number: |
NDA020950 |
| Labeler: |
EON LABS, INC. |
| Substance Name: |
ALBUTEROL SULFATE; IPRATROPIUM BROMIDE |
| Active Numerator Strength: |
3; .5 |
| Active Ingredient Unit: |
mg/3mL; mg/3mL |
| Pharm Classes: |
Anticholinergic [EPC],Cholinergic Antagonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
| DEA Schedule: |
|
