"42708-008-30" National Drug Code (NDC)

Amlodipine Besylate 30 TABLET in 1 BOTTLE (42708-008-30)
(QPharma Inc)

NDC Code42708-008-30
Package Description30 TABLET in 1 BOTTLE (42708-008-30)
Product NDC42708-008
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20070710
Marketing Category NameANDA
Application NumberANDA076846
ManufacturerQPharma Inc
Substance NameAMLODIPINE BESYLATE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

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