NDC 21695-014-30 - 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
21695-014-30
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 9 of 12 · 235 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BaclofenBACLOFENChartwell RX, LLC2a75db96-590a-43cf-aefb-3bbcb287dbf02024-10-10Warnings, Adverse reactionsExact identifier
rxcui: 197391
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENNCS HealthCare of KY, LLC dba Vangard Labsea4ad5c5-207c-4a68-8e6e-4ff101777e5c2024-10-04Warnings, Adverse reactionsExact identifier
unii: H789N3FKE8
BaclofenBACLOFENProficient Rx LPb981eb16-a195-41da-a186-3e91b63b2def2024-10-01Warnings, Adverse reactionsExact identifier
rxcui: 197391
unii: H789N3FKE8
BaclofenBACLOFENProficient Rx LP9d5a10cf-9a99-41eb-b4b8-9cf4cfaff6fc2024-10-01Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BACLOFENBACLOFENBryant Ranch Prepackf9c6d75a-a956-47b6-a5a2-deaf9797e2b22024-09-16Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENBryant Ranch Prepack08a6866f-b127-482f-9f22-113175487bdd2024-09-12Warnings, Adverse reactionsExact identifier
rxcui: 197391
unii: H789N3FKE8
BaclofenBACLOFENBryant Ranch Prepack5b92b0a6-ebba-4815-8b94-f2014674399b2024-09-05Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENBryant Ranch Prepack4634093b-6def-41d6-a7f3-23040125c4f42024-09-03Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENBryant Ranch Prepack655db2a3-daf7-4f4b-8f64-4a6d81fdc1652024-09-03Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENBryant Ranch Prepackb5fde991-7d12-4083-a3d6-363718f1f6a12024-08-16Warnings, Adverse reactionsExact identifier
rxcui: 197391
unii: H789N3FKE8
BaclofenBACLOFENZydus Lifesciences Limitedbb5c6faa-2933-44d1-8706-8302150be7342024-08-12Warnings, Adverse reactionsExact identifier
rxcui: 197391
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENZydus Pharmaceuticals (USA) Inc.cfc49176-8d01-4c39-9319-604dd087065c2024-08-12Warnings, Adverse reactionsExact identifier
rxcui: 197391
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENNuCare Pharmaceuticals,Inc.b2be2e6c-a247-30f4-e053-2a95a90a6ccb2024-07-17Warnings, Adverse reactionsExact identifier
rxcui: 197391
unii: H789N3FKE8
BaclofenBACLOFENDirect_rx1bf59c3b-f8eb-972e-e063-6394a90aeccc2024-06-28Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
Artificial TearsPOLYVINYL ALCOHOL, POVIDONENuCare Pharmaceuticals,Inc.9c1c4911-908e-3c3c-e053-2995a90abcfc2024-06-14WarningsExact identifier
unii: FZ989GH94E
BACLOFENBACLOFENBryant Ranch Prepack9834e409-8633-4f99-8ac7-7fa298d01c442024-05-30Warnings, Adverse reactionsExact identifier
rxcui: 197391
unii: H789N3FKE8
BaclofenBACLOFENAdvanced Rx Pharmacy of Tennessee, LLC19b049cf-56a4-aeaa-e063-6394a90a366d2024-05-30Warnings, Adverse reactionsExact identifier
rxcui: 197391
unii: H789N3FKE8
BACLOFENBACLOFENBryant Ranch Prepackadc072b9-e48b-470d-9eb1-fd7b52c1f1222024-05-29Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8
BACLOFENBACLOFENTruPharma LLC68aa591e-ea98-4438-9a4a-4f7e9ea2b2852024-04-17Warnings, Adverse reactionsExact identifier
rxcui: 197391
rxcui: 197392
unii: H789N3FKE8
BaclofenBACLOFENBryant Ranch Prepackd24135b3-e247-412f-a10b-ceecbdee3aef2024-04-02Warnings, Adverse reactionsExact identifier
rxcui: 197392
unii: H789N3FKE8

Reported adverse events (FAERS/openFDA)#

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