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"61919-705-60" National Drug Code (NDC)
Metoprolol Tartrate 60 TABLET, FILM COATED in 1 BOTTLE (61919-705-60)
(Direct_Rx)
NDC Code
61919-705-60
Package Description
60 TABLET, FILM COATED in 1 BOTTLE (61919-705-60)
Product NDC
61919-705
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
20190719
Marketing Category Name
ANDA
Application Number
ANDA077739
Manufacturer
Direct_Rx
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/61919-705-60