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"68462-211-90" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE (68462-211-90)
(Glenmark Generics Inc., USA)

NDC Code68462-211-90
Package Description90 TABLET in 1 BOTTLE (68462-211-90)
Product NDC68462-211
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20090408
Marketing Category NameANDA
Application NumberANDA078552
ManufacturerGlenmark Generics Inc., USA
Substance NameAMLODIPINE BESYLATE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68462-211-90





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