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Metoprolol Tartrate - 21695-298-90 - (Metoprolol tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 21695-298
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: 21695-298
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074644
Marketing Category: ANDA
Start Marketing Date: 19961210

Package Information of Metoprolol Tartrate

Package NDC: 21695-298-90
Package Description: 90 TABLET in 1 BOTTLE (21695-298-90)

NDC Information of Metoprolol Tartrate

NDC Code 21695-298-90
Proprietary Name Metoprolol Tartrate
Package Description 90 TABLET in 1 BOTTLE (21695-298-90)
Product NDC 21695-298
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19961210
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
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


General Information