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Albuterol Sulfate
Albuterol Sulfate - 54868-1073-3 - (Albuterol Sulfate)
Drug Information of Albuterol Sulfate
| Product NDC: | 54868-1073 |
| Proprietary Name: | Albuterol Sulfate |
| Non Proprietary Name: | Albuterol Sulfate |
| Active Ingredient(s): | 2.4 mg/1 & nbsp; Albuterol Sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Albuterol Sulfate
| Product NDC: | 54868-1073 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072637 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19930813 |
Package Information of Albuterol Sulfate
| Package NDC: | 54868-1073-3 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (54868-1073-3) |
NDC Information of Albuterol Sulfate
| NDC Code | 54868-1073-3 |
| Proprietary Name | Albuterol Sulfate |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (54868-1073-3) |
| Product NDC | 54868-1073 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Albuterol Sulfate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19930813 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ALBUTEROL SULFATE |
| Strength Number | 2.4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
