NDC 63629-3208

Sulindac

Sulindac

Sulindac is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Sulindac.

Product ID63629-3208_0b6d0c70-ae17-4788-b8d8-4ceebad00d88
NDC63629-3208
Product TypeHuman Prescription Drug
Proprietary NameSulindac
Generic NameSulindac
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1990-04-03
Marketing CategoryANDA / ANDA
Application NumberANDA071795
Labeler NameBryant Ranch Prepack
Substance NameSULINDAC
Active Ingredient Strength200 mg/1
Pharm ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 63629-3208-1

30 TABLET in 1 BOTTLE (63629-3208-1)
Marketing Start Date2006-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-3208-4 [63629320804]

Sulindac TABLET
Marketing CategoryANDA
Application NumberANDA071795
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-12-27
Inactivation Date2020-01-31

NDC 63629-3208-1 [63629320801]

Sulindac TABLET
Marketing CategoryANDA
Application NumberANDA071795
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-12-27
Inactivation Date2020-01-31

NDC 63629-3208-3 [63629320803]

Sulindac TABLET
Marketing CategoryANDA
Application NumberANDA071795
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-12-27
Inactivation Date2020-01-31

NDC 63629-3208-5 [63629320805]

Sulindac TABLET
Marketing CategoryANDA
Application NumberANDA071795
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-12-27
Inactivation Date2020-01-31

NDC 63629-3208-2 [63629320802]

Sulindac TABLET
Marketing CategoryANDA
Application NumberANDA071795
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SULINDAC200 mg/1

OpenFDA Data

SPL SET ID:d150c3f3-c267-4d48-9502-4700670c954b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198239
    • PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
    • NUI Code
  • N0000000160
  • N0000175722
  • N0000175721

    • Pharmacological Class

    • Cyclooxygenase Inhibitors [MoA]
    • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
    • Nonsteroidal Anti-inflammatory Drug [EPC]
    • Anti-Inflammatory Agents
    • Non-Steroidal [CS]

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

    NDCBrand NameGeneric Name
    0378-0427Sulindacsulindac
    0378-0531Sulindacsulindac
    0591-5660SulindacSulindac
    0591-5661SulindacSulindac
    0904-6216SulindacSulindac
    0904-6217SulindacSulindac
    23155-005SulindacSulindac
    23155-006SulindacSulindac
    24658-770SULINDACSULINDAC
    24658-771SULINDACSULINDAC
    33261-100SulindacSulindac
    42806-011SULINDACSULINDAC
    42806-018SULINDACSULINDAC
    50090-0528SulindacSulindac
    50090-0529SULINDACSULINDAC
    50090-2093SULINDACsulindac
    50090-4976SulindacSulindac
    51079-667Sulindacsulindac
    52959-195SulindacSulindac
    53489-478SULINDACsulindac
    53489-479SULINDACsulindac
    68151-2871SulindacSulindac
    68151-2872SulindacSulindac
    71335-0535SULINDACSULINDAC
    71335-0413SULINDACSULINDAC
    53808-0302SULINDACSULINDAC
    53808-0303SulindacSulindac
    54738-902SulindacSulindac
    53808-0814SulindacSulindac
    53808-0799SulindacSulindac
    54738-903SulindacSulindac
    55289-930SulindacSulindac
    55700-682SULINDACSULINDAC
    60429-697SULINDACSULINDAC
    60429-698SULINDACSULINDAC
    63629-3208SulindacSulindac
    70934-550SulindacSulindac
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