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"70518-1979-2" National Drug Code (NDC)
Metoprolol Tartrate 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1979-2)
(REMEDYREPACK INC.)
NDC Code
70518-1979-2
Package Description
180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1979-2)
Product NDC
70518-1979
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
20190326
Marketing Category Name
ANDA
Application Number
ANDA077739
Manufacturer
REMEDYREPACK INC.
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/70518-1979-2