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Albuterol Sulfate
Albuterol Sulfate - 21695-350-16 - (Albuterol Sulfate)
Drug Information of Albuterol Sulfate
| Product NDC: | 21695-350 |
| Proprietary Name: | Albuterol Sulfate |
| Non Proprietary Name: | Albuterol Sulfate |
| Active Ingredient(s): | 2 mg/5mL & nbsp; Albuterol Sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Albuterol Sulfate
| Product NDC: | 21695-350 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074749 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980130 |
Package Information of Albuterol Sulfate
| Package NDC: | 21695-350-16 |
| Package Description: | 473 mL in 1 BOTTLE (21695-350-16) |
NDC Information of Albuterol Sulfate
| NDC Code | 21695-350-16 |
| Proprietary Name | Albuterol Sulfate |
| Package Description | 473 mL in 1 BOTTLE (21695-350-16) |
| Product NDC | 21695-350 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Albuterol Sulfate |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 19980130 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | ALBUTEROL SULFATE |
| Strength Number | 2 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
