NDC 0121-0747

Sucralfate

Sucralfate

Sucralfate is a Oral Suspension in the Human Prescription Drug category. It is labeled and distributed by Pharmaceutical Associates, Inc.. The primary component is Sucralfate.

Product ID0121-0747_7d3ef177-eaad-da92-e053-2a91aa0a0070
NDC0121-0747
Product TypeHuman Prescription Drug
Proprietary NameSucralfate
Generic NameSucralfate
Dosage FormSuspension
Route of AdministrationORAL
Marketing Start Date2009-11-19
Marketing CategoryNDA / NDA
Application NumberNDA019183
Labeler NamePharmaceutical Associates, Inc.
Substance NameSUCRALFATE
Active Ingredient Strength1 g/10mL
Pharm ClassesAluminum Complex [EPC],Organometallic Compounds [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0121-0747-00

10 TRAY in 1 CASE (0121-0747-00) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (0121-0747-10)
Marketing Start Date2009-11-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0121-0747-30 [00121074730]

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

NDC 0121-0747-10 [00121074710]

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

NDC 0121-0747-40 [00121074740]

Sucralfate SUSPENSION
Marketing CategoryNDA
Application NumberNDA019183
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2020-04-28

NDC 0121-0747-00 [00121074700]

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

NDC 0121-0747-50 [00121074750]

Sucralfate SUSPENSION
Marketing CategoryNDA
Application NumberNDA019183
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-04-29

Drug Details

Active Ingredients

IngredientStrength
SUCRALFATE1 g/10mL

OpenFDA Data

SPL SET ID:fa6e4661-1bee-4a64-b982-9d44dbdb8498
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 313123

    • Pharmacological Class

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