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"52125-252-02" National Drug Code (NDC)
Metoprolol Succinate 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-252-02)
(REMEDYREPACK INC.)
NDC Code
52125-252-02
Package Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-252-02)
Product NDC
52125-252
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Metoprolol Succinate
Non-Proprietary Name
Metoprolol Succinate
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20130617
Marketing Category Name
ANDA
Application Number
ANDA090615
Manufacturer
REMEDYREPACK INC.
Substance Name
METOPROLOL SUCCINATE
Strength
100
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/52125-252-02