FDA.reportPublic FDA data

NDC 72162-2139-01 - 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
72162-2139
Requested NDC
72162-2139-01
Package NDCs from labels
72162-2139-1, 72162-2139-2, 72162-2139-3, 72162-2139-5, 72162-2139-9, 72162-2139-01
Manufacturer
Bryant Ranch Prepack
Effective date
2024-10-18
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Gabapentin - Bryant Ranch PrepackBryant Ranch Prepack2024-10-18HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-2139-1Gabapentin100 in 1 BOTTLE, PLASTICCAPSULE100104
72162-2139-2Gabapentin270 in 1 BOTTLE, PLASTICCAPSULE270104
72162-2139-3Gabapentin30 in 1 BOTTLE, PLASTICCAPSULE30104
72162-2139-5Gabapentin500 in 1 BOTTLE, PLASTICCAPSULE500104
72162-2139-9Gabapentin90 in 1 BOTTLE, PLASTICCAPSULE90104

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-2139GABAPENTIN CAPSULE [BRYANT RANCH PREPACK]104Current NDC, 5 package rows20241020_fb0b6613-57d6-4e24-946f-f5f87c460cf0.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-2139-2EA - Each72162-2139959de511-1021-424c-a488-7c80b2e5c31612024-08-12
72162-2139-3EA - Each72162-213929a74d58-02c3-42ba-81b6-676eecd6227f12024-12-10
72162-2139-5EA - Each72162-2139864bc7d6-425f-4ffb-8d01-2f06fab2cdc112024-02-14
72162-2139-9EA - Each72162-213929bb6581-6045-4996-a5de-c1970517301112024-12-10

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 81 of 301 · 6,004 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GabapentinGABAPENTINA-S Medication Solutions2343e3a1-82d0-4c70-a086-a01a0ce81ef32026-02-09Warnings, Adverse reactionsExact identifier
unii: 6CW7F3G59X
GabapentinGABAPENTINA-S Medication Solutions67330eef-c976-4862-b1ae-20f30f43df762026-02-09Warnings, Adverse reactionsExact identifier
unii: 6CW7F3G59X
AlcoholISOPROPYL ALCOHOLA-S Medication Solutions6b8834be-0235-4f7c-8d52-c2f6aa2d30492026-02-08WarningsExact identifier
unii: ND2M416302
Hampton Sun SPF 50 MineralZINC OXIDE 19.5% TITANIUM DIOXIDE 4.00%S&C Hampton Sun LLCd6c33436-042e-44e8-8b55-98be6e2468792026-02-06WarningsExact identifier
unii: 15FIX9V2JP
SHISEIDO WASO COLOR-SMART DAY MOISTURIZEROCTINOXATE, TITANIUM DIOXIDEShiseido Americas Corporationf291f077-1c72-48fc-bb19-c20bdeaaa5962026-02-06WarningsExact identifier
unii: 15FIX9V2JP
Hand SanitizerALCOHOLRetail Business Services, LLC8ba8176f-ddbd-48d7-bb62-74a499ea667c2026-02-06Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Advanced Hand SanitizerETHYL ALCOHOLRetail Business Services, LLC135ae232-3be4-4bbe-98fd-65eef3a675ad2026-02-06Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
SHISEIDO WASO COLOR-SMART DAY MOISTURIZEROCTINOXATE, TITANIUM DIOXIDEShiseido Americas Corporation54f63dd8-e77f-42e4-a6d3-61ab7beecf502026-02-06WarningsExact identifier
unii: 15FIX9V2JP
Advanced Hand SanitizerALCOHOLSalado Sales Inc.2869f574-e74c-492c-b3fa-b256b468746b2026-02-06Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
GABAPENTINGABAPENTINBryant Ranch Prepack2e331641-ec26-4d76-b16b-a9863c767afe2026-02-06Warnings, Adverse reactionsExact identifier
unii: 6CW7F3G59X
SEYTU Body SunscreenTITANIUM DIOXIDE AND ZINC OXIDEOmnilife USA, Inc.c411e9a6-b2ea-446b-a886-b92c61736e6c2026-02-05WarningsExact identifier
unii: 15FIX9V2JP
SEYTU Facial SunscreenTITANIUM DIOXIDE AND ZINC OXIDEOmnilife USA, Inc.96fd37fb-c3ff-413f-b2c8-50754f320ecc2026-02-05WarningsExact identifier
unii: 15FIX9V2JP
70% RubbingISOPROPYL ALCOHOLWalgreens Co.6ad37d18-5c19-4b5f-8313-edd430f84fb02026-02-05Warnings, Adverse reactionsExact identifier
unii: ND2M416302
Isopropyl AlcoholISOPROPYL ALCOHOLWalgreens Co.1473e6e4-dc5f-43d9-a249-111a181e3f762026-02-05Warnings, Adverse reactionsExact identifier
unii: ND2M416302
ForPro Premium Sterile Antiseptic Isopropyl Alcohol PadsISOPROPYL ALCOHOLTng workdwide6cc2ccae-b288-473e-a736-0974c96dbb892026-02-05WarningsExact identifier
unii: ND2M416302
Hand Sanitizer Cherry PopALCOHOLScent Theory Products LLC4a18b475-fd3b-10a3-e063-6294a90a4f472026-02-05WarningsExact identifier
unii: 3K9958V90M
Hand Sanitizer Ocean SplashALCOHOLScent Theory Products LLC4a18d7b2-94ca-7924-e063-6394a90af3d12026-02-05WarningsExact identifier
unii: 3K9958V90M
Hand Sanitizer Banana CremeALCOHOLScent Theory Products LLC4a18e8e0-43e3-70d8-e063-6294a90adf4b2026-02-05WarningsExact identifier
unii: 3K9958V90M
Hand Sanitizer Juicy PearALCOHOLScent Theory Products LLC4a18e8e0-43e5-70d8-e063-6294a90adf4b2026-02-05WarningsExact identifier
unii: 3K9958V90M
Hand Sanitizer Pink MelonALCOHOLScent Theory Products LLC4a18ec9c-d466-63c1-e063-6294a90a11222026-02-05WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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