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"0603-2338-32" National Drug Code (NDC)

Acetaminophen And Codeine 1000 TABLET in 1 BOTTLE, PLASTIC (0603-2338-32)
(Par Pharmaceutical, Inc.)

NDC Code0603-2338-32
Package Description1000 TABLET in 1 BOTTLE, PLASTIC (0603-2338-32)
Product NDC0603-2338
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAcetaminophen And Codeine
Non-Proprietary NameAcetaminophen And Codeine Phosphate
Dosage FormTABLET
UsageORAL
Start Marketing Date19880930
End Marketing Date20220228
Marketing Category NameANDA
Application NumberANDA089805
ManufacturerPar Pharmaceutical, Inc.
Substance NameACETAMINOPHEN; CODEINE PHOSPHATE
Strength300; 30
Strength Unitmg/1; mg/1
Pharmacy ClassesFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA ScheduleCIII

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0603-2338-32





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