NDC 50268-775

Trimethoprim

Trimethoprim

Trimethoprim is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Avpak. The primary component is Trimethoprim.

Product ID50268-775_7e7c1773-8851-74d1-e053-2a91aa0a490e
NDC50268-775
Product TypeHuman Prescription Drug
Proprietary NameTrimethoprim
Generic NameTrimethoprim
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2013-07-31
Marketing End Date2019-03-31
Marketing CategoryANDA /
Application NumberANDA070049
Labeler NameAvPAK
Substance NameTRIMETHOPRIM
Active Ingredient Strength100 mg/1
Pharm ClassesDihydrofolate R
NDC Exclude FlagN

Packaging

NDC SPL Data Element Entries

NDC 50268-775-15 [50268077515]

Trimethoprim TABLET
Marketing CategoryANDA
Application NumberANDA070049
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-07-31
Marketing End Date2019-03-31

NDC 50268-775-11 [50268077511]

Trimethoprim TABLET
Marketing CategoryANDA
Application NumberANDA070049
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-10-29
Marketing End Date2019-03-31

Drug Details

Medicade Reported Pricing

50268077515 TRIMETHOPRIM 100 MG TABLET

Pricing Unit: EA | Drug Type:

50268077511 TRIMETHOPRIM 100 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Trimethoprim" or generic name "Trimethoprim"

NDCBrand NameGeneric Name
0591-5571TrimethoprimTrimethoprim
40032-330TrimethoprimTrimethoprim
42291-845Trimethoprimtrimethoprim
43386-330TrimethoprimTrimethoprim
50268-775TrimethoprimTrimethoprim
51407-257TrimethoprimTrimethoprim
51862-486TrimethoprimTrimethoprim
55289-746TrimethoprimTrimethoprim
63629-7731TrimethoprimTrimethoprim
68151-2010TrimethoprimTrimethoprim
70954-541TrimethoprimTrimethoprim

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