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Metoprolol Tartrate - 0615-3552-05 - (Metoprolol tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 0615-3552
Proprietary Name: Metoprolol Tartrate
Non Proprietary Name: Metoprolol tartrate
Active Ingredient(s): 50    mg/1 & nbsp;   Metoprolol tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol Tartrate

Product NDC: 0615-3552
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074644
Marketing Category: ANDA
Start Marketing Date: 19970701

Package Information of Metoprolol Tartrate

Package NDC: 0615-3552-05
Package Description: 15 TABLET in 1 BLISTER PACK (0615-3552-05)

NDC Information of Metoprolol Tartrate

NDC Code 0615-3552-05
Proprietary Name Metoprolol Tartrate
Package Description 15 TABLET in 1 BLISTER PACK (0615-3552-05)
Product NDC 0615-3552
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970701
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name METOPROLOL TARTRATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol Tartrate


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