NDC 0006-0117

NDC 0006-0117

NDC 0006-0117 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0006-0117
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0006-0117-80 [00006011780]

SINGULAIR TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020829
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-02-20
Marketing End Date2013-09-19

NDC 0006-0117-28 [00006011728]

SINGULAIR TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020829
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-02-20
Marketing End Date2014-07-28

NDC 0006-0117-15 [00006011715]

SINGULAIR TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020829
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-01-15
Marketing End Date2014-11-30

NDC 0006-0117-54 [00006011754]

SINGULAIR TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020829
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-02-20
Marketing End Date2014-06-10

NDC 0006-0117-01 [00006011701]

SINGULAIR TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020829
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-02-20
Marketing End Date2014-07-28

NDC 0006-0117-31 [00006011731]

SINGULAIR TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA020829
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1998-02-20
Marketing End Date2014-06-10

Drug Details

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