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levalbuterol hydrochloride
levalbuterol hydrochloride - 0591-2918-23 - (levalbuterol hydrochloride)
Drug Information of levalbuterol hydrochloride
| Product NDC: | 0591-2918 |
| Proprietary Name: | levalbuterol hydrochloride |
| Non Proprietary Name: | levalbuterol hydrochloride |
| Active Ingredient(s): | .31 mg/3mL & nbsp; levalbuterol hydrochloride |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of levalbuterol hydrochloride
| Product NDC: | 0591-2918 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020837 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120820 |
Package Information of levalbuterol hydrochloride
| Package NDC: | 0591-2918-23 |
| Package Description: | 2 POUCH in 1 CARTON (0591-2918-23) > 12 VIAL, SINGLE-DOSE in 1 POUCH (0591-2918-39) > 3 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of levalbuterol hydrochloride
| NDC Code | 0591-2918-23 |
| Proprietary Name | levalbuterol hydrochloride |
| Package Description | 2 POUCH in 1 CARTON (0591-2918-23) > 12 VIAL, SINGLE-DOSE in 1 POUCH (0591-2918-39) > 3 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0591-2918 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levalbuterol hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20120820 |
| Marketing Category Name | NDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | LEVALBUTEROL HYDROCHLORIDE |
| Strength Number | .31 |
| Strength Unit | mg/3mL |
| Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
