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"0603-2108-32" National Drug Code (NDC)

Amlodipine Besylate 1000 TABLET in 1 BOTTLE, PLASTIC (0603-2108-32)
(Par Pharmaceutical)

NDC Code0603-2108-32
Package Description1000 TABLET in 1 BOTTLE, PLASTIC (0603-2108-32)
Product NDC0603-2108
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20100407
End Marketing Date20190430
Marketing Category NameANDA
Application NumberANDA078414
ManufacturerPar Pharmaceutical
Substance NameAMLODIPINE BESYLATE
Strength2.5
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/0603-2108-32





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