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#

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 12 of 12 · 235 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GABAPENTINGABAPENTINProficient Rx LP4bae5032-f634-4d1e-b672-8a7e2bd6a5fa2019-11-01Warnings, Adverse reactionsExact identifier
rxcui: 310430
GABAPENTINGABAPENTINProficient Rx LP92c4d589-533b-4fe4-833f-dd68cc1f7e662019-11-01Warnings, Adverse reactionsExact identifier
rxcui: 310432
GabapentinGABAPENTINProficient Rx LP2ef99c3d-866a-438b-a340-8beba8d4c4572019-11-01Warnings, Adverse reactionsExact identifier
rxcui: 310431
GabapentinGABAPENTINEpic Pharma, LLC030e656a-e384-49ac-830f-32140c18112d2019-01-07Warnings, Adverse reactionsExact identifier
rxcui: 310430
rxcui: 310432
rxcui: 310431
GABAPENTINGABAPENTINAphena Pharma Solutions - Tennessee, LLCa900bafb-8f49-4a01-ba7f-4fb228ec02532018-11-12Warnings, Adverse reactionsExact identifier
rxcui: 310431
GABAPENTINGABAPENTINAphena Pharma Solutions - Tennessee, LLC6702ed8f-4aaf-46fa-bf39-db75154aa44c2018-10-19Warnings, Adverse reactionsExact identifier
rxcui: 310432
GabapentinGABAPENTINAphena Pharma Solutions - Tennessee, LLC1b73e9db-eddb-49ba-9778-01d39ece4d162018-09-21Warnings, Adverse reactionsExact identifier
rxcui: 310431
GabapentinGABAPENTINAphena Pharma Solutions - Tennessee, LLCf455b415-12a2-4916-b826-246976a8af442018-09-12Warnings, Adverse reactionsExact identifier
rxcui: 310431
GabapentinGABAPENTINAphena Pharma Solutions - Tennessee, LLC5fbd601f-df95-4a79-a7d3-c3505e23b9132018-09-06Warnings, Adverse reactionsExact identifier
rxcui: 310430
GABAPENTINGABAPENTINAphena Pharma Solutions - Tennessee, LLC9d1b9121-c25a-4d28-91c5-5fc72f1167f42018-07-12Exact identifier
rxcui: 310431
GabapentinGABAPENTINAphena Pharma Solutions - Tennessee, LLC37d4d465-19a5-46db-80dc-0b7334b3343a2018-06-25Warnings, Adverse reactionsExact identifier
rxcui: 310430
GabapentinGABAPENTINAphena Pharma Solutions - Tennessee, LLC6fc8e8b2-5d0e-4c72-9a46-6d312c3efac72018-05-14Warnings, Adverse reactionsExact identifier
rxcui: 310432
GabapentinGABAPENTINAphena Pharma Solutions - Tennessee, LLC86b30e64-fe56-42b3-a0f8-d9ef5d4b8c492016-06-20Warnings, Adverse reactionsExact identifier
rxcui: 310432
rxcui: 310431
GabapentinGABAPENTINBi-Coastal Pharma International LLCe0cd96d1-b1ef-46ec-a5a3-9505b0811b8b2016-04-17Warnings, Adverse reactionsExact identifier
rxcui: 310430
rxcui: 310432
rxcui: 310431
A36432F9-BDDD-4B22-BE6D-ED6AC2B3846AA36432F9-BDDD-4B22-BE6D-ED6AC2B3846A2007-01-17Warnings, Adverse reactionsExact identifier
spl id: A36432F9-BDDD-4B22-BE6D-ED6AC2B3846A
spl set id: A36432F9-BDDD-4B22-BE6D-ED6AC2B3846A

Reported adverse events (FAERS/openFDA)#

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