NDC 72162-2139-05 - 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
72162-2139-05
Package NDCs from labels
72162-2139-1, 72162-2139-2, 72162-2139-3, 72162-2139-5, 72162-2139-9, 72162-2139-05
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 217 of 297 · 5,936 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CLE CCC Golden MediumTITANIUM DIOXIDE, OCTINOXATE, OCTISALATEKW ABSC, INC.de50e956-a014-4147-922b-63c95fa6f86b2024-12-19WarningsExact identifier
unii: 15FIX9V2JP
CLE CCC Neutral LightTITANIUM DIOXIDE, OCTINOXATE, OCTISALATEKW ABSC, INC.44cbb226-83ed-401b-baf8-ca8e4740dbef2024-12-19WarningsExact identifier
unii: 15FIX9V2JP
CLE CCC Neutral Medium LightTITANIUM DIOXIDE, OCTINOXATE, OCTISALATEKW ABSC, INC.615f5e39-695d-41d4-af59-e0d3b76789bb2024-12-19WarningsExact identifier
unii: 15FIX9V2JP
CLE CCC Warm DeepTITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, AVOBENZONEKW ABSC, INC.6ab3e360-8104-4439-93fb-e11bc4a775582024-12-19WarningsExact identifier
unii: 15FIX9V2JP
CLE CCC Neutral MediumTITANIUM DIOXIDE, OCTINOXATE, OCTISALATEKW ABSC, INC.a297ff64-678c-4936-8384-022606a2f33c2024-12-19WarningsExact identifier
unii: 15FIX9V2JP
CLE CCC Neutral FairTITANIUM DIOXIDE, OCTINOXATE, OCTISALATEKW ABSC, INC.aa8176c6-f1c9-43dd-96e0-f7d6ed30a1a22024-12-19WarningsExact identifier
unii: 15FIX9V2JP
CLE CCC Cool Medium DeepTITANIUM DIOXIDE, OCTINOXATE, OCTISALATEKW ABSC, INC.2e0365f9-d3c6-4404-90ac-772a829b3ade2024-12-19WarningsExact identifier
unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18- D2 NUTMEGOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDECOSMAX USA, INC29abae8f-53db-b592-e063-6294a90adabb2024-12-19WarningsExact identifier
unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 MOCHAOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDECOSMAX USA, INC29aba80c-55b7-b8d9-e063-6294a90a5cc12024-12-19WarningsExact identifier
unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 COCOAOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDECOSMAX USA, INC29abe97b-e9b3-6e27-e063-6294a90ae3ed2024-12-19WarningsExact identifier
unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 DEEP GOLDENOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDECOSMAX USA, INC29abdf3c-fb54-a5e3-e063-6394a90af4502024-12-19WarningsExact identifier
unii: 15FIX9V2JP
CeraVe Developed with Dermatologists Hydrating Mineral Sunscreen Broad Spectrum SPF 30 Face Sheer Tint SunscreenTITANIUM DIOXIDE AND ZINC OXIDEL'Oreal USA Products, Inc.f2e34230-7bfb-455f-8b33-6bff96fd9f0a2024-12-19WarningsExact identifier
unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 SHELLOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDECOSMAX USA, INC29868d60-b900-e0ad-e063-6294a90af87a2024-12-18WarningsExact identifier
unii: 15FIX9V2JP
Isopropyl alcohol 91 percentISOPROPYL ALCOHOLJell Pharmaceuticals Pvt. Ltd.cd98812b-017a-2cd2-e053-2a95a90a38ce2024-12-18WarningsExact identifier
unii: ND2M416302
Isopropyl Rubbing Alcohol 50%ISOPROPYL ALCOHOLMY IMPORTS LLCd4d72406-067d-1f67-e053-2995a90a1a9f2024-12-18WarningsExact identifier
unii: ND2M416302
AMORAY 70% ISOPROPYL RUBBING ALCOHOLISOPROPYL ALCOHOLMY IMPORT USA INC7114b527-106b-4629-867c-63dba13635a22024-12-18WarningsExact identifier
unii: ND2M416302
AMERICAN REDCROSS 70% ISOPROPYL RUBBING ALCOHOL WITH WINTERGREENISOPROPYL ALCOHOLMY IMPORTS USA LLCd4d7e7f8-7c8a-2b51-e053-2995a90a63d02024-12-18WarningsExact identifier
unii: ND2M416302
ISOPROPYL RUBBING ALCOHOL 50% WITH WINTERGREENISOPROPYL ALCOHOLMy Imports USA, LLCd4d77ec3-4930-74f0-e053-2a95a90a962a2024-12-18WarningsExact identifier
unii: ND2M416302
91% Isopropyl Rubbing AlcoholISOPROPYL ALCOHOLMY IMPORTS USA LLCd4d7adaf-c0fd-82fa-e053-2995a90ab9f62024-12-18WarningsExact identifier
unii: ND2M416302
ISOPROPYL RUBBING ALCOHOL 50% WITH WINTERGREENISOPROPYL ALCOHOLMY IMPORTS USA, LLCde47bf08-f64e-781d-e053-2a95a90ab08f2024-12-18WarningsExact identifier
unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

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