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METOPROLOL SUCCINATE - 43063-210-30 - (Metoprolol succinate)

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Drug Information of METOPROLOL SUCCINATE

Product NDC: 43063-210
Proprietary Name: METOPROLOL SUCCINATE
Non Proprietary Name: Metoprolol succinate
Active Ingredient(s): 25    mg/1 & nbsp;   Metoprolol succinate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of METOPROLOL SUCCINATE

Product NDC: 43063-210
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019962
Marketing Category: NDA
Start Marketing Date: 20110721

Package Information of METOPROLOL SUCCINATE

Package NDC: 43063-210-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-210-30)

NDC Information of METOPROLOL SUCCINATE

NDC Code 43063-210-30
Proprietary Name METOPROLOL SUCCINATE
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-210-30)
Product NDC 43063-210
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol succinate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110721
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name METOPROLOL SUCCINATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of METOPROLOL SUCCINATE


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