NDC 0185-0701

NDC 0185-0701

NDC 0185-0701 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0185-0701
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0185-0701-30 [00185070130]

Bisoprolol Fumarate and Hydrochlorothiazide TABLET, COATED
Marketing CategoryANDA
Application NumberANDA075579
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-09-25
Marketing End Date2016-10-31

NDC 0185-0701-05 [00185070105]

Bisoprolol Fumarate and Hydrochlorothiazide TABLET, COATED
Marketing CategoryANDA
Application NumberANDA075579
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-09-25
Marketing End Date2016-10-31

NDC 0185-0701-01 [00185070101]

Bisoprolol Fumarate and Hydrochlorothiazide TABLET, COATED
Marketing CategoryANDA
Application NumberANDA075579
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-09-25
Marketing End Date2017-04-30

Drug Details

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