NDC 50090-1572

Acetaminophen and Codeine

Acetaminophen And Codeine

Acetaminophen and Codeine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Acetaminophen; .

Product ID50090-1572_28352af4-39a4-4e32-b00b-74415cf0f9cc
NDC50090-1572
Product TypeHuman Prescription Drug
Proprietary NameAcetaminophen and Codeine
Generic NameAcetaminophen And Codeine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2008-05-29
Marketing CategoryANDA / ANDA
Application NumberANDA040779
Labeler NameA-S Medication Solutions
Substance NameACETAMINOPHEN;
Active Ingredient Strength300 mg/1; mg/1
Pharm ClassesFull Opioid Ago
DEA ScheduleCIII
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 50090-1572-4

30 TABLET in 1 BOTTLE (50090-1572-4)
Marketing Start Date2014-12-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50090-1572-1 [50090157201]

Acetaminophen and Codeine TABLET
Marketing CategoryANDA
Application NumberANDA040779
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-12-23
Marketing End Date2019-12-31

NDC 50090-1572-2 [50090157202]

Acetaminophen and Codeine TABLET
Marketing CategoryANDA
Application NumberANDA040779
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-12-23
Marketing End Date2019-12-31

NDC 50090-1572-7 [50090157207]

Acetaminophen and Codeine TABLET
Marketing CategoryANDA
Application NumberANDA040779
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-12-23
Marketing End Date2019-12-31

NDC 50090-1572-3 [50090157203]

Acetaminophen and Codeine TABLET
Marketing CategoryANDA
Application NumberANDA040779
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-12-23
Marketing End Date2019-12-31

NDC 50090-1572-4 [50090157204]

Acetaminophen and Codeine TABLET
Marketing CategoryANDA
Application NumberANDA040779
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-12-23
Marketing End Date2019-12-31

NDC 50090-1572-0 [50090157200]

Acetaminophen and Codeine TABLET
Marketing CategoryANDA
Application NumberANDA040779
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-12-23
Marketing End Date2019-04-30

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN300 mg/1

Pharmacological Class

  • Full Opioid Agonists [MoA]
  • Opioid Agonist [EPC]

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

NDCBrand NameGeneric Name
0440-7026Acetaminophen And Codeineacetaminophen and codeine phosphate
0440-7027Acetaminophen And Codeineacetaminophen and codeine phosphate
0603-2337Acetaminophen And Codeineacetaminophen and codeine phosphate
0603-2338Acetaminophen And Codeineacetaminophen and codeine phosphate
0603-2339Acetaminophen And Codeineacetaminophen and codeine phosphate
10544-100Acetaminophen and Codeineacetaminophen and codeine phosphate
33261-001Acetaminophen And Codeineacetaminophen and codeine phosphate
33261-002Acetaminophen And Codeineacetaminophen and codeine phosphate
33358-002Acetaminophen And Codeineacetaminophen and codeine phosphate
43353-010Acetaminophen and CodeineAcetaminophen and Codeine
50090-1572Acetaminophen and CodeineAcetaminophen and Codeine
50090-1573Acetaminophen and CodeineAcetaminophen and Codeine
50090-1574Acetaminophen and CodeineAcetaminophen and Codeine
50436-3227Acetaminophen and CodeineAcetaminophen and Codeine
51655-802ACETAMINOPHEN AND CODEINECodeine Phosphate and APAP
51655-808Acetaminophen and CodeineAcetaminophen and Codeine
52959-003Acetaminophen And Codeineacetaminophen and codeine phosphate
52959-446Acetaminophen and Codeineacetaminophen and codeine phosphate
53002-0101Acetaminophen and CodeineAcetaminophen and Codeine
53489-159ACETAMINOPHEN AND CODEINEAcetaminophen and Codeine Phosphate
53489-160ACETAMINOPHEN AND CODEINEAcetaminophen and Codeine Phosphate
53489-161ACETAMINOPHEN AND CODEINEAcetaminophen and Codeine Phosphate
61919-023ACETAMINOPHEN AND CODEINEACETAMINOPHEN AND CODEINE
61919-472ACETAMINOPHEN AND CODEINEACETAMINOPHEN AND CODEINE
61919-484ACETAMINOPHEN AND CODEINEACETAMINOPHEN AND CODEINE
61919-905ACETAMINOPHEN AND CODEINEACETAMINOPHEN AND CODEINE
63187-470Acetaminophen And Codeineacetaminophen and codeine phosphate
68071-3059Acetaminophen and CodeineAcetaminophen and Codeine
68387-250Acetaminophen And CodeineAcetaminophen And Codeine
68788-9403Acetaminophen and CodeineAcetaminophen and Codeine
68788-9259Acetaminophen And CodeineAcetaminophen And Codeine
71335-0545Acetaminophen and CodeineAcetaminophen and Codeine
63187-491Acetaminophen and CodeineAcetaminophen and Codeine
65162-033Acetaminophen and CodeineAcetaminophen and Codeine
66267-001Acetaminophen and CodeineAcetaminophen and Codeine
66267-759Acetaminophen and CodeineAcetaminophen and Codeine
66336-059Acetaminophen And CodeineAcetaminophen And Codeine
67046-902Acetaminophen And CodeineAcetaminophen And Codeine
67046-908Acetaminophen and CodeineAcetaminophen and Codeine
67296-0544Acetaminophen And CodeineAcetaminophen And Codeine
67544-882Acetaminophen And CodeineAcetaminophen And Codeine
67544-474Acetaminophen And CodeineAcetaminophen And Codeine
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.