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"57237-101-99" National Drug Code (NDC)
Metoprolol Tartrate 1000 TABLET, FILM COATED in 1 BOTTLE (57237-101-99)
(Rising Pharma Holdings, Inc.)
NDC Code
57237-101-99
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (57237-101-99)
Product NDC
57237-101
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Metoprolol Tartrate
Non-Proprietary Name
Metoprolol Tartrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20070911
Marketing Category Name
ANDA
Application Number
ANDA077739
Manufacturer
Rising Pharma Holdings, Inc.
Substance Name
METOPROLOL TARTRATE
Strength
50
Strength Unit
mg/1
Pharmacy Classes
Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57237-101-99