| NDC Code | 70518-1722-0 |
|---|
| Package Description | 2 POUCH in 1 CARTON (70518-1722-0) > 30 VIAL in 1 POUCH > 3 mL in 1 VIAL |
|---|
| Product NDC | 70518-1722 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ipratropium Bromide And Albuterol Sulfate |
|---|
| Non-Proprietary Name | Ipratropium Bromide And Albuterol Sulfate |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | RESPIRATORY (INHALATION) |
|---|
| Start Marketing Date | 20181210 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202496 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | IPRATROPIUM BROMIDE; ALBUTEROL SULFATE |
|---|
| Strength | .5; 2.5 |
|---|
| Strength Unit | mg/3mL; mg/3mL |
|---|
| Pharmacy Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
|---|