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"68180-721-09" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE (68180-721-09)
(Lupin Pharmaceuticals, Inc.)

NDC Code68180-721-09
Package Description90 TABLET in 1 BOTTLE (68180-721-09)
Product NDC68180-721
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20180815
Marketing Category NameANDA
Application NumberANDA078043
ManufacturerLupin Pharmaceuticals, Inc.
Substance NameAMLODIPINE BESYLATE
Strength10
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68180-721-09





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