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 106 of 301 · 6,004 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dr.Jart Premium Beauty Balm Fair-LightZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATEHave & Be Co., Ltd.b38b1b64-b433-4e11-9cf6-2108a552d1392025-12-31WarningsExact identifier
unii: 15FIX9V2JP
Dr.Jart Premium Beauty Balm Light Medium-MediumZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATEHave & Be Co., Ltd.45b1c2c6-a45b-4a45-bec9-e5341079c0a12025-12-31WarningsExact identifier
unii: 15FIX9V2JP
Dr.Jart Premium Beauty Balm Medium-TanZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATEHave & Be Co., Ltd.28a2ba45-1eff-488c-aae4-362b9f78b8df2025-12-31WarningsExact identifier
unii: 15FIX9V2JP
Dr.Jart Premium Beauty Balm Deep Tan-DeepZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATEHave & Be Co., Ltd.3c346960-b76b-4241-a188-8ee6948530782025-12-31WarningsExact identifier
unii: 15FIX9V2JP
DR.JART CICAPAIR TIGER GRASS CAMO DROPSZINC OXIDE, TITANIUM DIOXIDEHave & Be Co., Ltd.f06348f5-4ebc-325b-e053-2a95a90ada522025-12-31WarningsExact identifier
unii: 15FIX9V2JP
DR.JART EVERY SUN DAY MINERAL SUN SCREENTITANIUM DIOXIDE, ZINC OXIDEHave & Be Co., Ltd.f06c31b4-da5f-6495-e053-2995a90ae67c2025-12-31WarningsExact identifier
unii: 15FIX9V2JP
ALMOST powder MAKEUP BROAD SPECTRUM SPF 18OCTINOXATE AND TITANIUM DIOXIDECLINIQUE LABORATORIES LLC402add6d-a81e-4c9e-aee1-4abeb480894f2025-12-31WarningsExact identifier
unii: 15FIX9V2JP
SSDC Alphasan Hand SanitizerALCOHOLEcolab Inc.bbb0f924-3224-47f0-85b2-ebe024f8f9582025-12-31WarningsExact identifier
unii: 3K9958V90M
Kay Alcohol Foam Hand SanitizerALCOHOLEcolab Inc.37429e8a-581d-443e-8e8a-71fbb53c7c562025-12-31WarningsExact identifier
unii: 3K9958V90M
QSR Hand SanitizerALCOHOLEcolab Inc.901abea4-b82e-43c7-a1ac-0cdc1555dbc22025-12-31WarningsExact identifier
unii: 3K9958V90M
Ecolab Retail Foaming Alcohol Hand SanitizerALCOHOLEcolab Inc.e3f6eb96-05fe-4b20-bb72-954cdc47ffcb2025-12-31WarningsExact identifier
unii: 3K9958V90M
FIRST MARK ULTRA HAND SANITIZERALCOHOLPerformance Food Group80a490b4-dae5-4851-b3e6-2e558cdc51e52025-12-30WarningsExact identifier
unii: 3K9958V90M
EcolabALCOHOLEcolab Inc.f8561810-9d12-4c05-a547-b41bbb5170a92025-12-30WarningsExact identifier
unii: 3K9958V90M
PureForceALCOHOLEcolab Inc.775ee6e6-b3f8-4b97-b2b1-6f3a2defc6962025-12-30WarningsExact identifier
unii: 3K9958V90M
XHC-79ETHYL ALCOHOLEcolab Inc.ac662ae2-3228-4cce-9a20-96e1c234c27a2025-12-30WarningsExact identifier
unii: 3K9958V90M
EcolabALCOHOLEcolab Inc.a02591df-f121-4b92-8d0a-d4ef5edce1192025-12-30WarningsExact identifier
unii: 3K9958V90M
HEB 70 Isopropyl Alcohol WipesISOPROPYL ALCOHOLHEB Grocery Companye8dd7f84-3690-4ab3-a21f-43bf66984f4b2025-12-30WarningsExact identifier
unii: ND2M416302
Signature Care Eye Drops High PerformancePOLYETHYLENE GLYCOL 400, PROPYLENE GLYCOLBetter Living Brands LLC6f1f4f58-3208-4b06-9afb-c4beeed093142025-12-30WarningsExact identifier
unii: 6DC9Q167V3
Target Lubricant Eye Drops High PerformancePOLYETHYLENE GLYCOL 400, PROPYLENE GLYCOLTarget Corporation6c449374-8847-4c4a-9073-1951ff31d4042025-12-30WarningsExact identifier
unii: 6DC9Q167V3
Target Lubricant Eye Drops High PerformancePOLYETHYLENE GLYCOL 400, PROPYLENE GLYCOLTarget Corporationddc15dac-fbd8-42fa-80db-79f49fc6b9eb2025-12-30WarningsExact identifier
unii: 6DC9Q167V3

Reported adverse events (FAERS/openFDA)#

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