NDC 0603-3079

NDC 0603-3079

NDC 0603-3079 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0603-3079
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0603-3079-32 [00603307932]

Cyclobenzaprine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077797
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-02-28
Marketing End Date2018-10-31

NDC 0603-3079-21 [00603307921]

Cyclobenzaprine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077797
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-02-28
Marketing End Date2018-10-31

NDC 0603-3079-02 [00603307902]

Cyclobenzaprine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077797
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-02-28
Marketing End Date2018-10-31

NDC 0603-3079-28 [00603307928]

Cyclobenzaprine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077797
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-02-28
Marketing End Date2018-10-31

NDC 0603-3079-10 [00603307910]

Cyclobenzaprine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077797
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-02-28
Marketing End Date2018-10-31

NDC 0603-3079-03 [00603307903]

Cyclobenzaprine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077797
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-02-28
Marketing End Date2018-10-31

NDC 0603-3079-04 [00603307904]

Cyclobenzaprine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077797
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-02-28
Marketing End Date2018-10-31

NDC 0603-3079-34 [00603307934]

Cyclobenzaprine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077797
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-02-28
Marketing End Date2018-10-31

Drug Details

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