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"0093-0734-10" National Drug Code (NDC)
Metoprolol Tartrate 1000 TABLET, FILM COATED in 1 BOTTLE (0093-0734-10)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-0734-10
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (0093-0734-10)
Product NDC
0093-0734
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
19950406
Marketing Category Name
ANDA
Application Number
ANDA074141
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
METOPROLOL TARTRATE
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/0093-0734-10