NDC 63629-7957

Sucralfate

Sucralfate

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

Product ID63629-7957_38ad6fa2-eae7-463f-a46c-b0c1b4988eda
NDC63629-7957
Product TypeHuman Prescription Drug
Proprietary NameSucralfate
Generic NameSucralfate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1996-11-11
Marketing CategoryANDA / ANDA
Application NumberANDA070848
Labeler NameBryant Ranch Prepack
Substance NameSUCRALFATE
Active Ingredient Strength1 g/1
Pharm ClassesAluminum Complex [EPC],Organometallic Compounds [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 63629-7957-1

30 TABLET in 1 BOTTLE (63629-7957-1)
Marketing Start Date2019-03-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-7957-1 [63629795701]

Sucralfate TABLET
Marketing CategoryANDA
Application NumberANDA070848
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-03-18

Drug Details

Active Ingredients

IngredientStrength
SUCRALFATE1 g/1

OpenFDA Data

SPL SET ID:39225ba4-817e-46f6-a02c-fa1c13e43af2
Manufacturer
UNII

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

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