FDA.reportPublic FDA data

NDC 70518-1760-05 - 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
70518-1760
Requested NDC
70518-1760-05
Package NDCs from labels
70518-1760-0, 70518-1760-1, 70518-1760-2, 70518-1760-3, 70518-1760-4, 70518-1760-5, 70518-1760-6, 70518-1760-7, 70518-1760-8, 70518-1760-9, 70518-1760-05
Manufacturer
REMEDYREPACK INC.
Effective date
2026-08-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Gabapentin - REMEDYREPACK INC.REMEDYREPACK INC.2026-08-21HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-1760-0Gabapentin30 in 1 BLISTER PACKCAPSULE3019
70518-1760-1Gabapentin90 in 1 BOTTLE, PLASTICCAPSULE9019
70518-1760-2Gabapentin60 in 1 BOTTLE, PLASTICCAPSULE6019
70518-1760-3Gabapentin30 in 1 BOTTLE, PLASTICCAPSULE3019
70518-1760-4Gabapentin30 in 1 BLISTER PACKCAPSULE3019
70518-1760-5Gabapentin60 in 1 BOTTLE, PLASTICCAPSULE6019
70518-1760-6Gabapentin90 in 1 BOTTLE, PLASTICCAPSULE9019
70518-1760-7Gabapentin180 in 1 BOTTLE, PLASTICCAPSULE18019
70518-1760-8Gabapentin120 in 1 BOTTLE, PLASTICCAPSULE12019
70518-1760-9Gabapentin30 in 1 BOTTLE, PLASTICCAPSULE3019

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-1760GABAPENTIN CAPSULE [REMEDYREPACK INC.]15Current NDC, Legacy NDC, 10 package rows20250228_d06380d0-c894-427e-b13e-5a8f9eb86a34.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70518-1760-6EA - Each70518-1760da011682-68b5-4905-9334-9a4c18f88dc512026-01-08
70518-1760-8EA - Each70518-17602f72ec2d-9291-4c1e-a1de-23423d7c15e612026-01-08
70518-1760-9EA - Each70518-176027c5fd9b-6a24-4b61-87b8-f38a485f487712025-12-16

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 122 · 2,435 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
unii: 6CW7F3G59X
GabapentinGABAPENTINREMEDYREPACK INC.167d8b87-506c-4293-9579-563feaa715832026-09-10Warnings, Adverse reactionsExact identifier
rxcui: 310431
unii: 6CW7F3G59X
GabapentinGABAPENTINClinical Solutions Wholesale, LLCb7f9a106-52c6-49e4-acf5-8fb07761ba4f2026-09-09Warnings, Adverse reactionsExact identifier
unii: 6CW7F3G59X
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30W Aesthetics5b0f2c8f-d6fa-5e25-e063-6394a90a084d2026-09-09WarningsExact identifier
unii: 15FIX9V2JP
GabapentinGABAPENTINNuCare Pharmaceuticals,Inc.d35cd5ac-5ed6-2405-e053-2995a90a69462026-09-03Warnings, Adverse reactionsExact identifier
rxcui: 310430
unii: 6CW7F3G59X
GABAPENTINGABAPENTINPHOENIX RX LLC5a85ea98-4211-54eb-e063-6294a90aff332026-09-02Warnings, Adverse reactionsExact identifier
unii: 6CW7F3G59X
GabapentinGABAPENTINREMEDYREPACK INC.3dac0d5f-6e65-4c58-9d2a-4f6910b2d4ef2026-09-01Warnings, Adverse reactionsExact identifier
rxcui: 310430
unii: 6CW7F3G59X
GABAPENTINGABAPENTINREMEDYREPACK INC.1373587e-807a-462a-bff6-8a7113ce9f0a2026-09-01Warnings, Adverse reactionsExact identifier
rxcui: 310430
unii: 6CW7F3G59X
GabapentinGABAPENTINREMEDYREPACK INC.78445dbf-c7cd-419f-a7be-72821e4966282026-08-28Warnings, Adverse reactionsExact identifier
application number: ANDA090858
rxcui: 310432
unii: 6CW7F3G59X
GabapentinGABAPENTINREMEDYREPACK INC.4615aaa7-73d4-4473-8f26-e7a982f8a1662026-08-27Warnings, Adverse reactionsExact identifier
rxcui: 310432
unii: 6CW7F3G59X
MZANK SUNSCREEN DAILY ULTIMATE PROTECTION SPF50SUNSCREEN SPF50Guangzhou Meixi Biotechnology Co., Ltd.5a0b4bd2-f6ad-35dc-e063-6294a90a8a662026-08-27WarningsExact identifier
unii: 15FIX9V2JP
GabapentinGABAPENTINBryant Ranch Prepack1af098ad-28b5-463f-8efa-24d70a77d64c2026-08-26Warnings, Adverse reactionsExact identifier
rxcui: 310431
unii: 6CW7F3G59X
GabapentinGABAPENTINBryant Ranch Prepack9a2658d5-9b0e-4921-b4c5-4c89f1630d692026-08-26Warnings, Adverse reactionsExact identifier
rxcui: 310430
unii: 6CW7F3G59X
MELAO Hydrating Lightweight SunscreenAVOBENZONE,ENSULIZOLE,HOMOSALATE,OCTISALATE,OCTOCRYLENE,TITANIUM DIOXIDEGuangdong Aimu Biological Technology Co., Ltd59eeaea1-d726-99f3-e063-6394a90aeea32026-08-26WarningsExact identifier
unii: 15FIX9V2JP
GabapentinGABAPENTINBryant Ranch Prepack43cbff48-8219-41ba-b67d-3ae4544b78bb2026-08-26Warnings, Adverse reactionsExact identifier
rxcui: 310432
unii: 6CW7F3G59X
Q Skin ScienceSUNSCREENInternational Cosmeceuticals, Inc59e4c3d0-ee4c-2350-e063-6394a90ac9d22026-08-25WarningsExact identifier
unii: 15FIX9V2JP
GABAPENTINGABAPENTINBryant Ranch Prepack4c22c3e6-2471-4b89-945b-f846c4d7884e2026-08-25Warnings, Adverse reactionsExact identifier
rxcui: 310431
unii: 6CW7F3G59X
MELAO zinc stick(GREEN)TITANIUM DIOXIDE,ZINC OXIDE,OCTOCRYLENEGuangzhou Haishi Biological Technology Co., Ltd.59c70c82-f7ff-9a04-e063-6294a90a7b3d2026-08-24WarningsExact identifier
unii: 15FIX9V2JP
SKIN-INFUSED FOUNDATION SPF 25/ Mineral sunscreen broad Spectrum SPF 25 01ZINC OXIDE, TITANIUM DIOXIDECosmuses Cosmetics (Ningbo) Co., Ltd.59d74e3f-e3fa-a7a9-e063-6294a90a76e52026-08-24WarningsExact identifier
unii: 15FIX9V2JP
GabapentinGABAPENTINREMEDYREPACK INC.d06380d0-c894-427e-b13e-5a8f9eb86a342026-08-21Warnings, Adverse reactionsExact identifier
application number: ANDA090858
ndc (package): 70518-1760-8
ndc (package): 70518-1760-6
ndc (package): 70518-1760-0
ndc (package): 70518-1760-2
ndc (package): 70518-1760-3
ndc (package): 70518-1760-9
ndc (package): 70518-1760-1
ndc (package): 70518-1760-7
ndc (package): 70518-1760-4
ndc (package): 70518-1760-5
ndc (product): 70518-1760
ndc11 (package): 70518176005
rxcui: 310431
spl id: 59908c27-3aaf-6fce-e063-6394a90a7e0e
spl set id: d06380d0-c894-427e-b13e-5a8f9eb86a34
unii: 6CW7F3G59X

Reported adverse events (FAERS/openFDA)#

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