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Levalbuterol
Levalbuterol - 0093-4145-64 - (Levalbuterol)
Drug Information of Levalbuterol
| Product NDC: | 0093-4145 |
| Proprietary Name: | Levalbuterol |
| Non Proprietary Name: | Levalbuterol |
| Active Ingredient(s): | .31 mg/3mL & nbsp; Levalbuterol |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levalbuterol
| Product NDC: | 0093-4145 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090297 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130426 |
Package Information of Levalbuterol
| Package NDC: | 0093-4145-64 |
| Package Description: | 6 POUCH in 1 CARTON (0093-4145-64) > 4 VIAL, SINGLE-DOSE in 1 POUCH (0093-4145-04) > 3 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Levalbuterol
| NDC Code | 0093-4145-64 |
| Proprietary Name | Levalbuterol |
| Package Description | 6 POUCH in 1 CARTON (0093-4145-64) > 4 VIAL, SINGLE-DOSE in 1 POUCH (0093-4145-04) > 3 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0093-4145 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levalbuterol |
| Dosage Form Name | SOLUTION |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20130426 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | LEVALBUTEROL HYDROCHLORIDE |
| Strength Number | .31 |
| Strength Unit | mg/3mL |
| Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
