"68788-1738-9" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE (68788-1738-9)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-1738-9
Package Description90 TABLET in 1 BOTTLE (68788-1738-9)
Product NDC68788-1738
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20100407
Marketing Category NameANDA
Application NumberANDA078414
ManufacturerPreferred Pharmaceuticals, Inc.
Substance NameAMLODIPINE BESYLATE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

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