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"53808-1117-1" National Drug Code (NDC)
Metoprolol Tartrate 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-1117-1)
(DOH CENTRAL PHARMACY)
NDC Code
53808-1117-1
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (53808-1117-1)
Product NDC
53808-1117
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
20150814
Marketing Category Name
ANDA
Application Number
ANDA200981
Manufacturer
DOH CENTRAL PHARMACY
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/53808-1117-1