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"68788-7393-3" National Drug Code (NDC)
Alendronate Sodium 1 TABLET in 1 BLISTER PACK (68788-7393-3)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-7393-3
Package Description
1 TABLET in 1 BLISTER PACK (68788-7393-3)
Product NDC
68788-7393
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Alendronate Sodium
Non-Proprietary Name
Alendronate Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160928
Marketing Category Name
ANDA
Application Number
ANDA075710
Manufacturer
Preferred Pharmaceuticals Inc.
Substance Name
ALENDRONATE SODIUM
Strength
70
Strength Unit
mg/1
Pharmacy Classes
Bisphosphonate [EPC],Diphosphonates [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-7393-3