| NDC Code | 0378-4122-01 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4122-01) |
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| Product NDC | 0378-4122 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Albuterol Sulfate |
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| Non-Proprietary Name | Albuterol Sulfate |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20070130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078092 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | ALBUTEROL SULFATE |
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| Strength | 4 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
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