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Albuterol Sulfate
Albuterol Sulfate - 68788-0134-2 - (Albuterol Sulfate)
Drug Information of Albuterol Sulfate
| Product NDC: | 68788-0134 |
| Proprietary Name: | Albuterol Sulfate |
| Non Proprietary Name: | Albuterol Sulfate |
| Active Ingredient(s): | .83 mg/mL & 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: | 68788-0134 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074880 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970917 |
Package Information of Albuterol Sulfate
| Package NDC: | 68788-0134-2 |
| Package Description: | 1 POUCH in 1 BOX (68788-0134-2) > 25 VIAL, SINGLE-DOSE in 1 POUCH > 3 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Albuterol Sulfate
| NDC Code | 68788-0134-2 |
| Proprietary Name | Albuterol Sulfate |
| Package Description | 1 POUCH in 1 BOX (68788-0134-2) > 25 VIAL, SINGLE-DOSE in 1 POUCH > 3 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 68788-0134 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Albuterol Sulfate |
| Dosage Form Name | SOLUTION |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 19970917 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | ALBUTEROL SULFATE |
| Strength Number | .83 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
