FDA.reportPublic FDA data

NDC 53489-286 - Gabapentin

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
53489-286
Package NDCs from labels
53489-286-07, 53489-286-06, 53489-286-01, 53489-286-03, 53489-286-05, 53489-286-10
Manufacturer
MUTUAL PHARMACEUTICAL COMPANY, INC.
Effective date
2007-01-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
GABAPENTIN CAPSULESMUTUAL PHARMACEUTICAL COMPANY, INC.2007-01-17HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53489-286-01Gabapentin100 in 1 BOTTLE, PLASTICCAPSULE1001
53489-286-03Gabapentin250 in 1 BOTTLE, PLASTICCAPSULE2501
53489-286-05Gabapentin500 in 1 BOTTLE, PLASTICCAPSULE5001
53489-286-06Gabapentin60 in 1 BOTTLE, PLASTICCAPSULE601
53489-286-07Gabapentin30 in 1 BOTTLE, PLASTICCAPSULE301
53489-286-10Gabapentin1000 in 1 BOTTLE, PLASTICCAPSULE10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53489-286GABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]16 package rows20070202_A36432F9-BDDD-4B22-BE6D-ED6AC2B3846A.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GabapentinACTIVE INGREDIENT6CW7F3G59XGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
GabapentinACTIVE MOIETY6CW7F3G59XGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
Corn starchINACTIVE INGREDIENTGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
D&C Red #33INACTIVE INGREDIENTGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
D&C Yellow #10INACTIVE INGREDIENTGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
D&C Yellow #10 LakeINACTIVE INGREDIENTGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
FD&C Blue #1INACTIVE INGREDIENTGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
FD&C Blue #2INACTIVE INGREDIENTGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
FD&C Red #40INACTIVE INGREDIENTGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
gelatinINACTIVE INGREDIENT2G86QN327LGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
talcINACTIVE INGREDIENT7SEV7J4R1UGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
titanium dioxideINACTIVE INGREDIENT15FIX9V2JPGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]1
yellow iron oxideINACTIVE INGREDIENTGABAPENTIN (GABAPENTIN) CAPSULE [MUTUAL PHARMACEUTICAL COMPANY, INC.]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 12 · 235 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
gabapentinGABAPENTINREMEDYREPACK INC.4a975ebe-ae0a-446a-8a3d-2ca325e28f932026-09-11Warnings, Adverse reactionsExact identifier
rxcui: 310432
GabapentinGABAPENTINREMEDYREPACK INC.167d8b87-506c-4293-9579-563feaa715832026-09-10Warnings, Adverse reactionsExact identifier
rxcui: 310431
GabapentinGABAPENTINNuCare Pharmaceuticals,Inc.d35cd5ac-5ed6-2405-e053-2995a90a69462026-09-03Warnings, Adverse reactionsExact identifier
rxcui: 310430
GABAPENTINGABAPENTINREMEDYREPACK INC.1373587e-807a-462a-bff6-8a7113ce9f0a2026-09-01Warnings, Adverse reactionsExact identifier
rxcui: 310430
GabapentinGABAPENTINREMEDYREPACK INC.78445dbf-c7cd-419f-a7be-72821e4966282026-08-28Warnings, Adverse reactionsExact identifier
rxcui: 310432
GabapentinGABAPENTINREMEDYREPACK INC.4615aaa7-73d4-4473-8f26-e7a982f8a1662026-08-27Warnings, Adverse reactionsExact identifier
rxcui: 310432
GabapentinGABAPENTINBryant Ranch Prepack1af098ad-28b5-463f-8efa-24d70a77d64c2026-08-26Warnings, Adverse reactionsExact identifier
rxcui: 310431
GabapentinGABAPENTINBryant Ranch Prepack9a2658d5-9b0e-4921-b4c5-4c89f1630d692026-08-26Warnings, Adverse reactionsExact identifier
rxcui: 310430
GabapentinGABAPENTINBryant Ranch Prepack43cbff48-8219-41ba-b67d-3ae4544b78bb2026-08-26Warnings, Adverse reactionsExact identifier
rxcui: 310432
GABAPENTINGABAPENTINBryant Ranch Prepack4c22c3e6-2471-4b89-945b-f846c4d7884e2026-08-25Warnings, Adverse reactionsExact identifier
rxcui: 310431
GabapentinGABAPENTINREMEDYREPACK INC.d06380d0-c894-427e-b13e-5a8f9eb86a342026-08-21Warnings, Adverse reactionsExact identifier
rxcui: 310431
GabapentinGABAPENTINREMEDYREPACK INC.7652adc6-1aad-4422-b85c-0c6b11c23b732026-08-21Warnings, Adverse reactionsExact identifier
rxcui: 310430
GabapentinGABAPENTINBryant Ranch Prepackf0e7a6c9-ae6c-4259-81ab-a37db54e3c802026-08-19Warnings, Adverse reactionsExact identifier
rxcui: 310432
gabapentinGABAPENTINNuCare Pharmaceuticals, Inc.596eb696-7696-202e-e063-6394a90a28442026-08-19Warnings, Adverse reactionsExact identifier
rxcui: 310431
GabapentinGABAPENTINBryant Ranch Prepackeb2f6784-e7be-41b6-871b-2c3c961664ab2026-08-19Warnings, Adverse reactionsExact identifier
rxcui: 310432
GabapentinGABAPENTINBryant Ranch Prepack8a781649-3271-47a6-995f-50f91141a48a2026-08-19Warnings, Adverse reactionsExact identifier
rxcui: 310430
GabapentinGABAPENTINBryant Ranch Prepack6670a64f-7f58-479f-b285-394abb753e2e2026-08-19Warnings, Adverse reactionsExact identifier
rxcui: 310431
GabapentinGABAPENTINBryant Ranch Prepackcb81fd89-b32b-4538-bf5c-ab02f65b34582026-08-07Warnings, Adverse reactionsExact identifier
rxcui: 310430
GabapentinGABAPENTINBryant Ranch Prepack691205ba-fa65-4bc9-ba20-7d361382cff92026-08-07Warnings, Adverse reactionsExact identifier
rxcui: 310431
GabapentinGABAPENTINBryant Ranch Prepack97e47698-97c9-4eb5-a108-5850c2aa28182026-08-07Warnings, Adverse reactionsExact identifier
rxcui: 310430

Reported adverse events (FAERS/openFDA)#

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