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"68788-6805-3" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BOTTLE, PLASTIC (68788-6805-3)
(Preferred Pharmaceutical Inc.)
NDC Code
68788-6805-3
Package Description
30 TABLET in 1 BOTTLE, PLASTIC (68788-6805-3)
Product NDC
68788-6805
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20161107
Marketing Category Name
ANDA
Application Number
ANDA203245
Manufacturer
Preferred Pharmaceutical Inc.
Substance Name
AMLODIPINE BESYLATE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-6805-3