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"0093-5171-44" National Drug Code (NDC)
Alendronate Sodium 4 BLISTER PACK in 1 BOX (0093-5171-44) > 1 TABLET in 1 BLISTER PACK (0093-5171-19)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-5171-44
Package Description
4 BLISTER PACK in 1 BOX (0093-5171-44) > 1 TABLET in 1 BLISTER PACK (0093-5171-19)
Product NDC
0093-5171
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Alendronate Sodium
Non-Proprietary Name
Alendronate Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20080206
End Marketing Date
20180531
Marketing Category Name
ANDA
Application Number
ANDA075710
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
ALENDRONATE SODIUM
Strength
70
Strength Unit
mg/1
Pharmacy Classes
Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-5171-44