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Metaproterenol Sulfate - 0603-1422-58 - (Metaproterenol Sulfate)

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Drug Information of Metaproterenol Sulfate

Product NDC: 0603-1422
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)

Labeler Information of Metaproterenol Sulfate

Product NDC: 0603-1422
Labeler Name: Qualitest Pharmaceuticals, Inc,
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073632
Marketing Category: ANDA
Start Marketing Date: 19920722

Package Information of Metaproterenol Sulfate

Package NDC: 0603-1422-58
Package Description: 473 mL in 1 BOTTLE, PLASTIC (0603-1422-58)

NDC Information of Metaproterenol Sulfate

NDC Code 0603-1422-58
Proprietary Name Metaproterenol Sulfate
Package Description 473 mL in 1 BOTTLE, PLASTIC (0603-1422-58)
Product NDC 0603-1422
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metaproterenol Sulfate
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 19920722
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals, Inc,
Substance Name METAPROTERENOL SULFATE
Strength Number 10
Strength Unit mg/5mL
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Metaproterenol Sulfate


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