NDC 50268-730

Sulfasalazine

Sulfasalazine

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

Product ID50268-730_79a09e27-5add-2bf2-e053-2991aa0a34b7
NDC50268-730
Product TypeHuman Prescription Drug
Proprietary NameSulfasalazine
Generic NameSulfasalazine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2014-01-14
Marketing CategoryANDA / ANDA
Application NumberANDA085828
Labeler NameAvPAK
Substance NameSULFASALAZINE
Active Ingredient Strength500 mg/1
Pharm ClassesAminosalicylate [EPC],Aminosalicylic Acids [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 50268-730-15

50 BLISTER PACK in 1 BOX (50268-730-15) > 1 TABLET in 1 BLISTER PACK (50268-730-11)
Marketing Start Date2014-01-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50268-730-11 [50268073011]

Sulfasalazine TABLET
Marketing CategoryANDA
Application NumberANDA085828
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-10-29

NDC 50268-730-15 [50268073015]

Sulfasalazine TABLET
Marketing CategoryANDA
Application NumberANDA085828
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-01-14

Drug Details

Active Ingredients

IngredientStrength
SULFASALAZINE500 mg/1

OpenFDA Data

SPL SET ID:67dcfa7d-f656-6c92-60bb-4b40dcecf080
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198232
  • Pharmacological Class

    • Aminosalicylate [EPC]
    • Aminosalicylic Acids [CS]
    • Aminosalicylate [EPC]
    • Aminosalicylic Acids [CS]

    Medicade Reported Pricing

    50268073015 SULFASALAZINE 500 MG TABLET

    Pricing Unit: EA | Drug Type:

    50268073011 SULFASALAZINE 500 MG TABLET

    Pricing Unit: EA | Drug Type:

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

    NDCBrand NameGeneric Name
    0093-3234SulfasalazineSulfasalazine
    0591-0796SulfasalazineSulfasalazine
    0603-5801Sulfasalazinesulfasalazine
    10544-288Sulfasalazinesulfasalazine
    23155-019SulfasalazineSulfasalazine
    33261-756Sulfasalazinesulfasalazine
    43353-495SulfasalazineSulfasalazine
    50090-0086SulfasalazineSulfasalazine
    50090-2013SulfasalazineSulfasalazine
    50268-730SulfasalazineSulfasalazine
    59762-0104SulfasalazineSulfasalazine
    68071-4215SulfasalazineSulfasalazine
    68788-9021SULFASALAZINESULFASALAZINE
    70518-0185SulfasalazineSulfasalazine
    70518-1829SulfasalazineSulfasalazine
    59762-5000SulfasalazineSulfasalazine
    63629-5688SulfasalazineSulfasalazine
    70518-2342SulfasalazineSulfasalazine
    0013-0101AzulfidineSulfasalazine
    0013-0102AzulfidineSulfasalazine

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