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"51079-782-20" National Drug Code (NDC)
Pravastatin Sodium 100 BLISTER PACK in 1 CARTON (51079-782-20) / 1 TABLET in 1 BLISTER PACK (51079-782-01)
(Mylan Institutional Inc.)
NDC Code
51079-782-20
Package Description
100 BLISTER PACK in 1 CARTON (51079-782-20) / 1 TABLET in 1 BLISTER PACK (51079-782-01)
Product NDC
51079-782
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pravastatin Sodium
Non-Proprietary Name
Pravastatin Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20071003
Marketing Category Name
ANDA
Application Number
ANDA076056
Manufacturer
Mylan Institutional Inc.
Substance Name
PRAVASTATIN SODIUM
Strength
40
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/51079-782-20