FDA.reportPublic FDA data

NDC 55530-030-10 - Ranitidine

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
55530-030
Requested NDC
55530-030-10
Package NDCs from labels
55530-030-06, 55530-030-01, 55530-030-05, 55530-030-10
Manufacturer
GENPHARM, L.P.
Effective date
2006-11-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
RANITIDINE TABLETS USPGENPHARM, L.P.2006-11-08Human prescription drug label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55530-030-01Ranitidine100 in 1 BOTTLETABLET, FILM COATED1001
55530-030-05Ranitidine500 in 1 BOTTLETABLET, FILM COATED5001
55530-030-06Ranitidine60 in 1 BOTTLETABLET, FILM COATED601
55530-030-10Ranitidine1000 in 1 BOTTLETABLET, FILM COATED10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55530-030RANITIDINE (RANITIDINE) TABLET, FILM COATED [GENPHARM, L.P.]14 package rows20061201_A7C056ED-BE64-4AFA-AD79-D90EA4352BED.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
RanitidineACTIVE INGREDIENT884KT10YB7RANITIDINE (RANITIDINE) TABLET, FILM COATED [GENPHARM, L.P.]1
RanitidineACTIVE MOIETY884KT10YB7RANITIDINE (RANITIDINE) TABLET, FILM COATED [GENPHARM, L.P.]1
croscarmellose sodiumINACTIVE INGREDIENTRANITIDINE (RANITIDINE) TABLET, FILM COATED [GENPHARM, L.P.]1
hydroxypropyl methylcelluloseINACTIVE INGREDIENTRANITIDINE (RANITIDINE) TABLET, FILM COATED [GENPHARM, L.P.]1
magnesium stearateINACTIVE INGREDIENT70097M6I30RANITIDINE (RANITIDINE) TABLET, FILM COATED [GENPHARM, L.P.]1
microcrystalline celluloseINACTIVE INGREDIENTRANITIDINE (RANITIDINE) TABLET, FILM COATED [GENPHARM, L.P.]1
polydextroseINACTIVE INGREDIENTRANITIDINE (RANITIDINE) TABLET, FILM COATED [GENPHARM, L.P.]1
polyethylene glycolINACTIVE INGREDIENTRANITIDINE (RANITIDINE) TABLET, FILM COATED [GENPHARM, L.P.]1
titanium dioxideINACTIVE INGREDIENT15FIX9V2JPRANITIDINE (RANITIDINE) TABLET, FILM COATED [GENPHARM, L.P.]1
triethyl citrateINACTIVE INGREDIENTRANITIDINE (RANITIDINE) TABLET, FILM COATED [GENPHARM, L.P.]1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 ยท 5 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RanitidineRANITIDINEAmneal Pharmaceuticals of New York LLCb38a3332-5c54-453f-aeb7-070f830955c22026-05-01Adverse reactionsExact identifier
rxcui: 198193
rxcui: 198191
RANITIDINERANITIDINERising Pharma Holdings, Inc.0fba6615-37c2-4ba6-b6e5-09599369a5bc2025-12-05Adverse reactionsExact identifier
rxcui: 198193
rxcui: 198191
RanitidineRANITIDINEGranules India Ltdaab81d9f-397d-49fb-8083-77a1872cc71f2025-12-02WarningsExact identifier
rxcui: 198191
RanitidineRANITIDINEDr. Reddy's Laboratories Limited00df8a42-296f-80dd-98af-ee8b30eb38cc2025-05-23WarningsExact identifier
rxcui: 198191
A7C056ED-BE64-4AFA-AD79-D90EA4352BEDA7C056ED-BE64-4AFA-AD79-D90EA4352BED2006-11-08Adverse reactionsExact identifier
spl id: A7C056ED-BE64-4AFA-AD79-D90EA4352BED
spl set id: A7C056ED-BE64-4AFA-AD79-D90EA4352BED

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.