NDC 33358-001

NDC 33358-001

NDC 33358-001 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 33358-001
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 33358-001-15 [33358000115]

Acetaminophen and Codeine TABLET
Marketing CategoryANDA
Application NumberANDA040779
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-05-29
Inactivation Date2020-01-31

NDC 33358-001-30 [33358000130]

Acetaminophen and Codeine TABLET
Marketing CategoryANDA
Application NumberANDA040779
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-05-29
Inactivation Date2020-01-31

NDC 33358-001-60 [33358000160]

Acetaminophen and Codeine TABLET
Marketing CategoryANDA
Application NumberANDA040779
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-05-29
Inactivation Date2020-01-31

NDC 33358-001-20 [33358000120]

Acetaminophen and Codeine TABLET
Marketing CategoryANDA
Application NumberANDA040779
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-05-29
Inactivation Date2020-01-31

Drug Details


© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.