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"68462-291-13" National Drug Code (NDC)
Linezolid 3 BLISTER PACK in 1 CARTON (68462-291-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Glenmark Pharmaceuticals Inc., USA)
NDC Code
68462-291-13
Package Description
3 BLISTER PACK in 1 CARTON (68462-291-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
68462-291
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Linezolid
Non-Proprietary Name
Linezolid
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20151221
Marketing Category Name
ANDA
Application Number
ANDA078987
Manufacturer
Glenmark Pharmaceuticals Inc., USA
Substance Name
LINEZOLID
Strength
600
Strength Unit
mg/1
Pharmacy Classes
Oxazolidinone Antibacterial [EPC],Oxazolidinones [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68462-291-13