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"68788-1737-9" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE (68788-1737-9)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-1737-9
Package Description90 TABLET in 1 BOTTLE (68788-1737-9)
Product NDC68788-1737
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
Strength10
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-1737-9





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