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METOPROLOL SUCCINATE - 0904-6170-05 - (METOPROLOL SUCCINATE)

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Drug Information of METOPROLOL SUCCINATE

Product NDC: 0904-6170
Proprietary Name: METOPROLOL SUCCINATE
Non Proprietary Name: METOPROLOL SUCCINATE
Active Ingredient(s): 50    mg/1 & nbsp;   METOPROLOL SUCCINATE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of METOPROLOL SUCCINATE

Product NDC: 0904-6170
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090615
Marketing Category: ANDA
Start Marketing Date: 20101005

Package Information of METOPROLOL SUCCINATE

Package NDC: 0904-6170-05
Package Description: 10 BOX, UNIT-DOSE in 1 CARTON (0904-6170-05) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0904-6170-61)

NDC Information of METOPROLOL SUCCINATE

NDC Code 0904-6170-05
Proprietary Name METOPROLOL SUCCINATE
Package Description 10 BOX, UNIT-DOSE in 1 CARTON (0904-6170-05) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0904-6170-61)
Product NDC 0904-6170
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METOPROLOL SUCCINATE
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101005
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name METOPROLOL SUCCINATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of METOPROLOL SUCCINATE


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