Application 085828

Type
ANDA
Sponsor
WATSON LABS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001SULFASALAZINESULFASALAZINETABLET;ORAL500MGNoNo

Orange Book products#

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A085828-001SULFASALAZINESULFASALAZINE500MGTABLET / ORALABApproved before 1982

Therapeutic equivalence codes#

Application-product, TE code table
Application-productTE code
A085828-001AB

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SulfasalazineSULFASALAZINEAmerican Health Packagingd967092f-9685-446b-b7b8-17821e29417b2026-07-27Warnings, Adverse reactionsExact identifier
SulfasalazineSULFASALAZINEBryant Ranch Prepack618c5324-d0a6-4d00-9b12-0de88a71c1802024-04-04Warnings, Adverse reactionsExact identifier
SulfasalazineSULFASALAZINETeva Pharmaceuticals USA, Inc.3c59593b-e1a5-47cb-a82b-3e5e492053442023-08-22Warnings, Adverse reactionsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

WARNINGS Hepatic, Renal, and Hematologic Toxicity or Other Conditions Only after critical appraisal should sulfasalazine tablets be given to patients with hepatic or renal damage or blood dyscrasias. Deaths associated with the administration of sulfasalazine have been reported from hypersensitivity reactions, agranulocytosis, aplastic anemia, other blood dyscrasias, renal and liver damage, irreversible neuromuscular and central nervous system changes, and fibrosing alveolitis. The presence of clinical signs such as sore throat, fever, pallor, purpura, or jaundice may be indications of serious blood disorders or hepatotoxicity. Complete blood counts, as well as urinalysis with careful microscopic examination, should be done frequently in patients receiving sulfasalazine (see PRECAUTIONS, Laboratory Tests ). Discontinue treatment with sulfasalazine while awaiting the results of blood tests. Discontinue sulfasalazine tablets if renal function deteriorates while on therapy. Oligospermia and Infertility Oligospermia and infertility have been observed in men treated with sulfasalazine; however, withdrawal of the drug appears to reverse these effects. Serious Infections Serious infections, including fatal sepsis and pneumonia, have been reported. Some infections were associated with agranulocytosis, neutropenia, or myelosuppression. Discontinue sulfasalazine tablets if a patient develops a serious infection. Closely monitor patients for the development of signs and symptoms of infection during and after treatment with sulfasalazine tablets. For a patient who develops a new infection during treatment with sulfasalazine tablets, perform a prompt and complete diagnostic workup for infection and myelosuppression. Caution should be exercised when considering the use of sulfasalazine in patients with a history of recurring or chronic infections or with underlying conditions or concomitant drugs which may predispose patients to infections. Hypersensitivity Reactions Severe hypersensitivity reactions may include internal organ involvement, such as hepatitis, nephritis, myocarditis, mononucleosis-like syndrome (i.e., pseudomononucleosis), hematological abnormalities (including hematophagic histiocytosis), and/or pneumonitis including eosinophilic infiltration. Severe Cutaneous Adverse Reactions Drug Reactions with Eosinophilia and Systemic Symptoms (DRESS) Severe, life-t...

Adverse reactions cross-check#

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adverse reactions

ADVERSE REACTIONS The most common adverse reactions associated with sulfasalazine are anorexia, headache, nausea, vomiting, gastric distress, and apparently reversible oligospermia. These occur in about one-third of the patients. Less frequent adverse reactions are skin rash, pruritus, urticaria, fever, Heinz body anemia, hemolytic anemia, and cyanosis, which may occur at a frequency of one in every thirty patients or less. Experience suggests that with a daily dosage of 4 g or more, or total serum sulfapyridine levels above 50 mcg/mL, the incidence of adverse reactions tends to increase. Although the listing which follows includes a few adverse reactions which have not been reported with this specific drug, the pharmacological similarities among the sulfonamides require that each of these reactions be considered when sulfasalazine tablets are administered. Less common or rare adverse reactions include: Blood dyscrasias: aplastic anemia, agranulocytosis, leukopenia, megaloblastic (macrocytic) anemia, purpura, thrombocytopenia, hypoprothrombinemia, methemoglobinemia, congenital neutropenia, and myelodysplastic syndrome. Hypersensitivity reactions: erythema multiforme, epidermal necrolysis (SJS/TEN) with corneal damage, exfoliative dermatitis, DRESS, anaphylaxis, serum sickness syndrome, interstitial lung disease, pneumonitis with or without eosinophilia, vasculitis, fibrosing alveolitis, pleurisy/pleuritis, pericarditis with or without tamponade, allergic myocarditis, polyarteritis nodosa, lupus erythematosus-like syndrome, hepatitis and hepatic necrosis with or without immune complexes, fulminant hepatitis, sometimes leading to liver transplantation, parapsoriasis varioliformis acuta (Mucha-Haberman syndrome), rhabdomyolysis, photosensitization, arthralgia, periorbital edema, conjunctival and scleral injection, and alopecia. Gastrointestinal reactions: hepatitis, hepatic failure, pancreatitis, bloody diarrhea, impaired folic acid absorption, impaired digoxin absorption, stomatitis, diarrhea, abdominal pains, and neutropenic enterocolitis. Central nervous system reactions: transverse myelitis, convulsions, meningitis, transient lesions of the posterior spinal column, cauda equina syndrome, Guillian-Barre syndrome, peripheral neuropathy, mental depression, vertigo, hearing loss, insomnia, ataxia, hallucinations, tinnitus, and drowsiness. Renal reactions: to...

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0093-3234SulfasalazineSulfasalazineTeva Pharmaceuticals USA, Inc.ANDACurrent
0591-0796SulfasalazineSulfasalazineActavis Pharma, Inc.ANDACurrent
0591-0796SulfasalazineSulfasalazineActavis Pharma, Inc.ANDACurrent
0591-0796SulfasalazineSulfasalazineActavis Pharma, Inc.ANDACurrent
0591-0796SulfasalazineSulfasalazineActavis Pharma, Inc.ANDACurrent
0591-0796SulfasalazineSulfasalazineActavis Pharma, Inc.ANDACurrent
50090-2013SulfasalazineSulfasalazineA-S Medication SolutionsANDACurrent
50090-2013SulfasalazineSulfasalazineA-S Medication SolutionsANDACurrent
50090-2013SulfasalazineSulfasalazineA-S Medication SolutionsANDACurrent
50268-730SulfasalazineSulfasalazineAvPAKANDACurrent
50268-730SulfasalazineSulfasalazineAvPAKANDACurrent
63629-5688SulfasalazineSulfasalazineBryant Ranch PrepackANDACurrent
63629-5688SulfasalazineSulfasalazineBryant Ranch PrepackANDACurrent
63629-5688SulfasalazineSulfasalazineBryant Ranch PrepackANDACurrent
63629-5688SulfasalazineSulfasalazineBryant Ranch PrepackANDACurrent
68071-4215SulfasalazineSulfasalazineNuCare Pharmaceuticals,Inc.ANDACurrent
68071-4215SulfasalazineSulfasalazineNuCare Pharmaceuticals,Inc.ANDACurrent
70518-0185SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
70518-0185SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
70518-0185SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
70518-0185SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
70518-0185SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
70518-0185SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
70518-0185SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
70518-2342SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
70518-2342SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
70518-2342SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
70518-2342SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
70518-2342SulfasalazineSulfasalazineREMEDYREPACK INC.ANDACurrent
71610-577SulfasalazineSulfasalazineAphena Pharma Solutions - Tennessee, LLCANDACurrent