NDC 55154-5778

Sucralfate

Sucralfate

Sucralfate is a Oral Suspension in the Human Prescription Drug category. It is labeled and distributed by Cardinal Health 107, Llc. The primary component is Sucralfate.

Product ID55154-5778_4b18a21f-5990-4cc1-b36b-953c3ad85e40
NDC55154-5778
Product TypeHuman Prescription Drug
Proprietary NameSucralfate
Generic NameSucralfate
Dosage FormSuspension
Route of AdministrationORAL
Marketing Start Date2009-11-19
Marketing End Date2023-06-30
Marketing CategoryNDA / NDA
Application NumberNDA019183
Labeler NameCardinal Health 107, LLC
Substance NameSUCRALFATE
Active Ingredient Strength1 g/10mL
Pharm ClassesAluminum Complex [EPC], Organometallic Compounds [CS]
NDC Exclude FlagN

Packaging

NDC 55154-5778-5

5 CUP, UNIT-DOSE in 1 BAG (55154-5778-5) > 10 mL in 1 CUP, UNIT-DOSE
Marketing Start Date2009-11-19
Marketing End Date2023-06-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55154-5778-5 [55154577805]

Sucralfate SUSPENSION
Marketing CategoryNDA
Application NumberNDA019183
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-11-19

Drug Details

Active Ingredients

IngredientStrength
SUCRALFATE1 g/10mL

OpenFDA Data

SPL SET ID:cafe60c5-ba29-4baa-bf4b-576df59a65b7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 313123
  • UPC Code
  • 0055154577854
  • Pharmacological Class

    • Aluminum Complex [EPC]
    • Organometallic Compounds [CS]

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

    NDCBrand NameGeneric Name
    0093-2210SucralfateSucralfate
    0121-0747SucralfateSucralfate
    0121-0974SucralfateSucralfate
    0254-1011SucralfateSucralfate
    0378-9205sucralfatesucralfate
    0591-0780SucralfateSucralfate
    0591-3892SucralfateSucralfate
    0615-4517SucralfateSucralfate
    0904-7269SucralfateSucralfate
    17856-0062SucralfateSucralfate Oral
    17856-1011SucralfateSucralfate
    29033-003SucralfateSucralfate
    42291-757SucralfateSucralfate
    42291-781SucralfateSucralfate Oral
    43353-061SucralfateSucralfate
    45865-845SucralfateSucralfate
    50090-0582SucralfateSucralfate
    50090-3019SucralfateSucralfate
    50090-5287SucralfateSucralfate
    50268-732SucralfateSucralfate Oral
    50268-745SucralfateSucralfate Oral
    51079-753SucralfateSucralfate
    51655-031SUCRALFATESUCRALFATE
    53002-4930SucralfateSucralfate
    53808-0593SucralfateSUCRALFATE
    53808-0797SucralfateSUCRALFATE
    55154-4057SucralfateSucralfate
    55154-4379SucralfateSucralfate
    68094-171SucralfateSucralfate
    68788-8946SucralfateSucralfate
    70518-0775SucralfateSucralfate
    71610-244SucralfateSucralfate
    71610-017SucralfateSucralfate
    76519-1025SUCRALFATESUCRALFATE
    55289-292SucralfateSucralfate
    59762-0401SucralfateSucralfate
    60429-297SucralfateSucralfate
    63629-6535SucralfateSucralfate
    63629-1307SucralfateSucralfate
    63739-943SucralfateSucralfate
    66267-596SucralfateSucralfate
    66689-790SucralfateSucralfate
    55154-8133SucralfateSucralfate
    63629-7957SucralfateSucralfate
    55154-5778SucralfateSucralfate
    65162-062SucralfateSucralfate
    68071-1749SucralfateSucralfate
    17856-0170CarafateSucralfate

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