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"52125-209-02" National Drug Code (NDC)
Metoprolol Tartrate 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-209-02)
(REMEDYREPACK INC.)
NDC Code
52125-209-02
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (52125-209-02)
Product NDC
52125-209
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
20130320
Marketing Category Name
ANDA
Application Number
ANDA078459
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/52125-209-02