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"68788-7679-9" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE, PLASTIC (68788-7679-9)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7679-9
Package Description90 TABLET in 1 BOTTLE, PLASTIC (68788-7679-9)
Product NDC68788-7679
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200402
Marketing Category NameANDA
Application NumberANDA203245
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameAMLODIPINE BESYLATE
Strength2.5
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/68788-7679-9





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