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Albuterol Sulfate
Albuterol Sulfate - 0378-6991-52 - (albuterol sulfate)
Drug Information of Albuterol Sulfate
| Product NDC: | 0378-6991 |
| Proprietary Name: | Albuterol Sulfate |
| Non Proprietary Name: | albuterol sulfate |
| Active Ingredient(s): | .75 mg/3mL & nbsp; albuterol sulfate |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Albuterol Sulfate
| Product NDC: | 0378-6991 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020949 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100129 |
Package Information of Albuterol Sulfate
| Package NDC: | 0378-6991-52 |
| Package Description: | 5 POUCH in 1 CARTON (0378-6991-52) > 5 VIAL in 1 POUCH > 3 mL in 1 VIAL |
NDC Information of Albuterol Sulfate
| NDC Code | 0378-6991-52 |
| Proprietary Name | Albuterol Sulfate |
| Package Description | 5 POUCH in 1 CARTON (0378-6991-52) > 5 VIAL in 1 POUCH > 3 mL in 1 VIAL |
| Product NDC | 0378-6991 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | albuterol sulfate |
| Dosage Form Name | SOLUTION |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20100129 |
| Marketing Category Name | NDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | ALBUTEROL SULFATE |
| Strength Number | .75 |
| Strength Unit | mg/3mL |
| Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
