Product NDC: | 54838-507 |
Proprietary Name: | Metaproterenol Sulfate |
Non Proprietary Name: | Metaproterenol Sulfate |
Active Ingredient(s): | 10 mg/5mL & nbsp; Metaproterenol Sulfate |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54838-507 |
Labeler Name: | Silarx Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA073632 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090908 |
Package NDC: | 54838-507-80 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (54838-507-80) |
NDC Code | 54838-507-80 |
Proprietary Name | Metaproterenol Sulfate |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (54838-507-80) |
Product NDC | 54838-507 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Metaproterenol Sulfate |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20090908 |
Marketing Category Name | ANDA |
Labeler Name | Silarx Pharmaceuticals, Inc |
Substance Name | METAPROTERENOL SULFATE |
Strength Number | 10 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |