NDC 0093-5172

NDC 0093-5172

NDC 0093-5172 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0093-5172
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0093-5172-44 [00093517244]

Alendronate Sodium TABLET
Marketing CategoryANDA
Application NumberANDA075710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-02-06
Marketing End Date2017-12-31

NDC 0093-5172-19 [00093517219]

Alendronate Sodium TABLET
Marketing CategoryANDA
Application NumberANDA075710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-02-06
Marketing End Date2017-12-31

NDC 0093-5172-29 [00093517229]

Alendronate Sodium TABLET
Marketing CategoryANDA
Application NumberANDA075710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-06-04
Marketing End Date2017-12-31

NDC 0093-5172-20 [00093517220]

Alendronate Sodium TABLET
Marketing CategoryANDA
Application NumberANDA075710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-02-06
Marketing End Date2014-03-31

Drug Details

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