NDC 0172-5664

NDC 0172-5664

NDC 0172-5664 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0172-5664
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0172-5664-60 [00172566460]

Buspirone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA075385
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-03-02
Marketing End Date2012-08-31

NDC 0172-5664-00 [00172566400]

Buspirone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA075385
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-08-26
Marketing End Date2012-08-31

NDC 0172-5664-10 [00172566410]

Buspirone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA075385
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-03-02
Marketing End Date2012-08-31

NDC 0172-5664-49 [00172566449]

Buspirone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA075385
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-03-02
Marketing End Date2012-03-16

NDC 0172-5664-80 [00172566480]

Buspirone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA075385
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-03-02
Marketing End Date2012-03-16

NDC 0172-5664-70 [00172566470]

Buspirone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA075385
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-03-02
Marketing End Date2012-08-31

Drug Details

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