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"31722-239-10" National Drug Code (NDC)

Amlodipine Besylate 1000 TABLET in 1 BOTTLE (31722-239-10)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-239-10
Package Description1000 TABLET in 1 BOTTLE (31722-239-10)
Product NDC31722-239
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20110101
Marketing Category NameANDA
Application NumberANDA077955
ManufacturerCamber 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/31722-239-10





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