FDA.reportPublic FDA data

Application 206822

Type
ANDA
Sponsor
PHARM ASSOC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDESOLUTION;ORAL100MG/5MLNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0121-0826OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDEPharmaceutical Associates, Inc.ANDACurrent
0121-0826OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDEPharmaceutical Associates, Inc.ANDACurrent
0121-0826OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDEPharmaceutical Associates, Inc.ANDACurrent
0121-0826OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDEPharmaceutical Associates, Inc.ANDACurrent
0121-0826OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDEPharmaceutical Associates, Inc.ANDACurrent
0121-0826OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDEPharmaceutical Associates, Inc.ANDACurrent
0121-0826OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDEPharmaceutical Associates, Inc.ANDACurrent
17856-0826OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDEATLANTIC BIOLOGICALS CORP.ANDACurrent

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
76144ORIG 2023-11-03
49574ORIG2017-08-29