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"13107-062-01" National Drug Code (NDC)
Metoprolol Tartrate 100 TABLET, FILM COATED in 1 BOTTLE (13107-062-01)
(Aurolife Pharma LLC)
NDC Code
13107-062-01
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (13107-062-01)
Product NDC
13107-062
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
20100917
Marketing Category Name
ANDA
Application Number
ANDA077739
Manufacturer
Aurolife Pharma LLC
Substance Name
METOPROLOL TARTRATE
Strength
25
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/13107-062-01