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"0093-7152-31" National Drug Code (NDC)
Simvastatin 1 BLISTER PACK in 1 CARTON (0093-7152-31) > 30 TABLET, FILM COATED in 1 BLISTER PACK
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-7152-31
Package Description
1 BLISTER PACK in 1 CARTON (0093-7152-31) > 30 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
0093-7152
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Simvastatin
Non-Proprietary Name
Simvastatin
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20060627
Marketing Category Name
ANDA
Application Number
ANDA076052
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
SIMVASTATIN
Strength
5
Strength Unit
mg/1
Pharmacy Classes
HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-7152-31