| NDC Code | 47335-753-52 |
|---|
| Package Description | 6 POUCH in 1 CARTON (47335-753-52) > 5 VIAL, SINGLE-DOSE in 1 POUCH > 3 mL in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 47335-753 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Levalbuterol Inhalation Solution |
|---|
| Non-Proprietary Name | Levalbuterol Inhalation Solution |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | RESPIRATORY (INHALATION) |
|---|
| Start Marketing Date | 20181201 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207820 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | LEVALBUTEROL HYDROCHLORIDE |
|---|
| Strength | 1.25 |
|---|
| Strength Unit | mg/3mL |
|---|
| Pharmacy Classes | Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC] |
|---|