NDC 49999-852

Oxycodone and Acetaminophen

Oxycodone And Acetaminophen

Oxycodone and Acetaminophen is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Quality Care Products Llc. The primary component is Acetaminophen; Oxycodone Hydrochloride.

Product ID49999-852_286cc1e8-9395-429a-b318-38d2290e798d
NDC49999-852
Product TypeHuman Prescription Drug
Proprietary NameOxycodone and Acetaminophen
Generic NameOxycodone And Acetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2010-06-10
Marketing CategoryANDA /
Application NumberANDA087463
Labeler NameQuality Care products LLC
Substance NameACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Active Ingredient Strength325 mg/1; mg/1
Pharm ClassesFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 49999-852-30

30 TABLET in 1 BOTTLE, PLASTIC (49999-852-30)
Marketing Start Date2022-08-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49999-852-40 [49999085240]

Oxycodone and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA087463
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-06-10
Marketing End Date2014-06-01

NDC 49999-852-00 [49999085200]

Oxycodone and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA087463
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-06-10
Marketing End Date2014-06-01

NDC 49999-852-90 [49999085290]

Oxycodone and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA087463
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-06-10
Marketing End Date2014-06-01

NDC 49999-852-15 [49999085215]

Oxycodone and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA087463
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-06-10
Marketing End Date2014-06-01

NDC 49999-852-30 [49999085230]

Oxycodone and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA087463
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-06-10
Marketing End Date2014-06-01

NDC 49999-852-60 [49999085260]

Oxycodone and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA087463
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-06-10
Marketing End Date2014-06-01

Drug Details

NDC Crossover Matching brand name "Oxycodone and Acetaminophen" or generic name "Oxycodone And Acetaminophen"

NDCBrand NameGeneric Name
0054-0551Oxycodone and AcetaminophenOxycodone and Acetaminophen
0228-2981Oxycodone and AcetaminophenOxycodone and Acetaminophen
0228-2982Oxycodone and AcetaminophenOxycodone and Acetaminophen
0228-2983Oxycodone and AcetaminophenOxycodone and Acetaminophen
0406-0512OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
0406-0522OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
0406-0523OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
0527-1669Oxycodone and AcetaminophenOxycodone and Acetaminophen
0527-1671Oxycodone and AcetaminophenOxycodone and Acetaminophen
0603-4978Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
0603-4979Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
0603-4982Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
0603-4998Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
68084-355Oxycodone and AcetaminophenOxycodone and Acetaminophen
68084-710Oxycodone and AcetaminophenOxycodone and Acetaminophen
68094-013Oxycodone and AcetaminophenOxycodone and Acetaminophen
68084-699Oxycodone and AcetaminophenOxycodone and Acetaminophen
68308-480Oxycodone and AcetaminophenOxycodone and Acetaminophen
68308-840Oxycodone and AcetaminophenOxycodone and Acetaminophen
68308-842Oxycodone and AcetaminophenOxycodone and Acetaminophen
68308-843Oxycodone and AcetaminophenOxycodone and Acetaminophen
68308-405Oxycodone and AcetaminophenOxycodone and Acetaminophen
68308-475Oxycodone and AcetaminophenOxycodone and Acetaminophen
68308-841Oxycodone and AcetaminophenOxycodone and Acetaminophen
70700-105Oxycodone and AcetaminophenOxycodone and Acetaminophen
70710-1327Oxycodone and AcetaminophenOxycodone and Acetaminophen
70710-1328Oxycodone and AcetaminophenOxycodone and Acetaminophen
70710-1329Oxycodone and AcetaminophenOxycodone and Acetaminophen
70710-1330Oxycodone and AcetaminophenOxycodone and Acetaminophen
71335-0146Oxycodone and AcetaminophenOxycodone and Acetaminophen
71335-0216Oxycodone and AcetaminophenOxycodone and Acetaminophen
71335-0193Oxycodone and AcetaminophenOxycodone and Acetaminophen
71335-0221oxycodone and acetaminophenoxycodone and acetaminophen
71335-1036Oxycodone and AcetaminophenOxycodone and Acetaminophen
71335-0316Oxycodone and AcetaminophenOxycodone and Acetaminophen
71335-0722Oxycodone and AcetaminophenOxycodone and Acetaminophen
0904-6438Oxycodone and AcetaminophenOxycodone and Acetaminophen
0904-6439Oxycodone and AcetaminophenOxycodone and Acetaminophen
0904-6437Oxycodone and AcetaminophenOxycodone and Acetaminophen
10544-287OXYCODONE AND ACETAMINOPHENOXYCODONE AND ACETAMINOPHEN
10702-187Oxycodone and AcetaminophenOxycodone and Acetaminophen
10544-621Oxycodone and AcetaminophenOxycodone and Acetaminophen
10702-238OXYCODONE AND ACETAMINOPHENOXYCODONE AND ACETAMINOPHEN
10702-185Oxycodone and AcetaminophenOxycodone and Acetaminophen
10702-186Oxycodone and AcetaminophenOxycodone and Acetaminophen
10702-184Oxycodone and AcetaminophenOxycodone and Acetaminophen
13107-044Oxycodone and AcetaminophenOxycodone and Acetaminophen
13107-043Oxycodone and AcetaminophenOxycodone and Acetaminophen
12634-942Oxycodone and AcetaminophenOxycodone and Acetaminophen
13107-045Oxycodone and AcetaminophenOxycodone and Acetaminophen

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