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"68180-751-03" National Drug Code (NDC)

Amlodipine Besylate 1000 TABLET in 1 BOTTLE (68180-751-03)
(Lupin Pharmaceuticals, Inc.)

NDC Code68180-751-03
Package Description1000 TABLET in 1 BOTTLE (68180-751-03)
Product NDC68180-751
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20070803
End Marketing Date20210731
Marketing Category NameANDA
Application NumberANDA078043
ManufacturerLupin Pharmaceuticals, Inc.
Substance NameAMLODIPINE BESYLATE
Strength5
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/68180-751-03





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