NDC 21695-014-60 - Baclofen

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
21695-014
Requested NDC
21695-014-60
Package NDCs from labels
21695-014-30, 21695-014-42, 21695-014-60, 21695-014-90, 21695-014-72
Manufacturer
Rebel Distributors Corp.
Effective date
2009-12-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Baclofen Tablets USP 10mg & 20mgRebel Distributors Corp.2009-12-01HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unitNational Council for Prescription Drug Programs2012-07-24Indexing - Billing Unit

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21695-014-30Baclofen30 in 1 BOTTLETABLET301
21695-014-42Baclofen42 in 1 BOTTLETABLET421
21695-014-60Baclofen60 in 1 BOTTLETABLET601
21695-014-72Baclofen120 in 1 BOTTLETABLET1201
21695-014-90Baclofen90 in 1 BOTTLETABLET901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21695-014BACLOFEN TABLET [REBEL DISTRIBUTORS CORP.]1Legacy NDC, 5 package rows20100329_d88886cc-62c0-44dd-8a3f-cac601832d8e.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
21695-014-30EA - Each21695-014045b5479-8a48-4d8c-9230-f5d2a183b56912012-07-24
21695-014-60EA - Each21695-014f974850f-d5fd-43d0-8ba4-4c7e7a27757712012-07-24
21695-014-72EA - Each21695-01467d2f2c6-d0bc-41c7-872b-eb0966b5425512012-07-24
21695-014-90EA - Each21695-01410ba6395-b45c-47ec-8f19-96e039588df312012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BACLOFENACTIVE INGREDIENTH789N3FKE8BACLOFEN TABLET [REBEL DISTRIBUTORS CORP.]1
BACLOFENACTIVE MOIETYH789N3FKE8BACLOFEN TABLET [REBEL DISTRIBUTORS CORP.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UBACLOFEN TABLET [REBEL DISTRIBUTORS CORP.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30BACLOFEN TABLET [REBEL DISTRIBUTORS CORP.]1
POVIDONEINACTIVE INGREDIENTFZ989GH94EBACLOFEN TABLET [REBEL DISTRIBUTORS CORP.]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJBACLOFEN TABLET [REBEL DISTRIBUTORS CORP.]1

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 7 of 12 · 235 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BaclofenBACLOFENBryant Ranch Prepacka748da19-d3eb-499e-986c-2043a1356f2b2025-07-15Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BACLOFENBACLOFENA-S Medication Solutionseb690a49-b87b-433f-9afe-2966406fe00e2025-07-15Warnings, Adverse reactionsExact identifier
rxcui: 197391
unii: H789N3FKE8
BACLOFENBACLOFENA-S Medication Solutionsaf0ade6c-9dd4-42d3-879e-4201fbe585ee2025-07-15Warnings, Adverse reactionsExact identifier
rxcui: 197391
unii: H789N3FKE8
BaclofenBACLOFENAphena Pharma Solutions - Tennessee, LLC39ad22ca-f034-f605-e063-6294a90a08e42025-07-11Warnings, Adverse reactionsExact identifier
rxcui: 197391
unii: H789N3FKE8
BaclofenBACLOFENAphena Pharma Solutions - Tennessee, LLC3981db3e-672c-1634-e063-6294a90a4cd12025-07-09Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENBryant Ranch Prepack3ac0f0d2-86d8-46d0-88e5-c243734b08142025-06-26Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BACLOFENBACLOFENAdvagen Pharma Ltd2a43830f-a28b-ca15-e063-6294a90a6b1a2025-06-12Warnings, Adverse reactionsExact identifier
unii: H789N3FKE8
BACLOFENBACLOFENHAWAII REPACK, INC.bc48a775-1feb-44c4-9453-e1ccf3d929bd2025-06-11Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENAdvagen Pharma Ltd.,75ab298b-b2a7-458f-accc-5bfc89b89a162025-06-11Warnings, Adverse reactionsExact identifier
unii: H789N3FKE8
BACLOFENBACLOFENAurobindo Pharma Limited4679a275-9307-4b0f-a2eb-2d83227ea84d2025-06-11Warnings, Adverse reactionsExact identifier
rxcui: 197391
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENSagent Pharmaceuticalsd4bfba33-9f4d-4c43-ae6c-bcf67ef8fe512025-05-05Boxed warning, Warnings, Adverse reactionsExact identifier
unii: H789N3FKE8
BACLOFENBACLOFENProficient Rx LP0243dd97-1d40-48f7-8853-76e046c605f22025-04-01Warnings, Adverse reactionsExact identifier
unii: H789N3FKE8
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U
BaclofenBACLOFENBryant Ranch Prepack8cb96e7b-9c40-46a9-b964-7a573b7a03422025-02-21Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
Walgreens Soothing Eye Relief Lubricant Eye DropsPOLYVINYL ALCOHOL, POVIDONEWalgreens Co.29b7387b-ad65-3a11-e063-6394a90a6a152025-02-14WarningsExact identifier
unii: FZ989GH94E
BACLOFENBACLOFENXLCare Pharmaceuticals Inc.2b4908fb-47b5-4675-be9e-ca1ad48a72522025-02-05Warnings, Adverse reactionsExact identifier
rxcui: 197391
rxcui: 197392
unii: H789N3FKE8
BACLOFENBACLOFENNuCare Pharmaceuticals,Inc.fd00fa8f-2797-c3f0-e053-6294a90a975f2025-02-05Warnings, Adverse reactionsExact identifier
rxcui: 197391
unii: H789N3FKE8
BACLOFENBACLOFENAdvanced Rx of Tennessee, LLC2cf71f5f-6d46-7506-e063-6294a90a186f2025-01-30Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENDirect_Rx020632f4-5e8a-f4a0-e063-6294a90a63012025-01-28Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENBryant Ranch Prepack4b215bc5-f7f9-4b39-b8ee-42b233ee4aa22025-01-22Warnings, Adverse reactionsExact identifier
rxcui: 197391
unii: H789N3FKE8

Reported adverse events (FAERS/openFDA)#

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