Product NDC: | 54868-3407 |
Proprietary Name: | Albuterol Sulfate |
Non Proprietary Name: | Albuterol Sulfate |
Active Ingredient(s): | 5 mg/mL & nbsp; Albuterol Sulfate |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-3407 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074543 |
Marketing Category: | ANDA |
Start Marketing Date: | 19941019 |
Package NDC: | 54868-3407-0 |
Package Description: | 1 BOTTLE, GLASS in 1 CARTON (54868-3407-0) > 20 mL in 1 BOTTLE, GLASS |
NDC Code | 54868-3407-0 |
Proprietary Name | Albuterol Sulfate |
Package Description | 1 BOTTLE, GLASS in 1 CARTON (54868-3407-0) > 20 mL in 1 BOTTLE, GLASS |
Product NDC | 54868-3407 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Albuterol Sulfate |
Dosage Form Name | SOLUTION |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 19941019 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | ALBUTEROL SULFATE |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |